New 2,3,4,5-tetrahydro-1h-pyrido [4,3-b] indole compounds and methods of use thereof

ABSTRACT

This disclosure relates to new tricyclic compounds that may be used to modulate a histamine receptor in an individual. Compounds are described, including new 2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole compounds. Pharmaceutical compositions comprising the compounds are also provided, as are methods of using the compounds in a variety of therapeutic applications, including the treatment of a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder and/or a neuronal disorder.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to U.S. Provisional Patent Application No. 61/062,430 filed Jan. 25, 2008, U.S. Provisional Patent Application No. 61/062,394 filed Jan. 25, 2008 and Russian Patent Application No. 2008102993 filed Jan. 25, 2008, the disclosures of each of which are incorporated herein by reference in their entireties.

STATEMENT OF RIGHTS TO INVENTIONS MADE UNDER FEDERALLY SPONSORED RESEARCH

Not applicable.

BACKGROUND OF THE INVENTION

Neurotransmitters such as histamine, serotonin, dopamine and norepinephrine mediate a large number of processes in the central nervous system (CNS) as well as outside the CNS. Abnormal neurotransmitter levels are associated with a wide variety of diseases and conditions including, but not limited to, Alzheimer's disease, Parkinson's Disease, autism, Guillain-Barré syndrome, mild cognitive impairment, schizophrenia, anxiety, multiple sclerosis, stroke, traumatic brain injury, spinal cord injury, diabetic neuropathy, fibromyalgia, bipolar disorders, psychosis, depression and a variety of allergic diseases. Compounds that modulate these neurotransmitters may be useful therapeutics.

Histamine receptors belong to the superfamily of G protein-coupled seven transmembrane proteins. G protein-coupled receptors constitute one of the major signal transduction systems in eukaryotic cells. Coding sequences for these receptors, in those regions believed to contribute to the agonist-antagonist binding site, are strongly conserved across mammalian species. Histamine receptors are found in most peripheral tissue and within the central nervous system. Compounds capable of modulating a histamine receptor may find use in therapy, e.g., as antihistamines.

Dimebon is a known anti-histamine drug that has also been characterized as a neuroprotective agent useful to treat, inter alia, neurodegenerative diseases. Dimebon has been shown to inhibit the death of brain cells (neurons) in preclinical models of Alzheimer's disease and Huntington's disease, making it a novel potential treatment for these and other neurodegenerative diseases. In addition, dimebon has been shown to improve the mitochondrial function of cells in the setting of cellular stress with very high potency. For example, dimebon treatment improved mitochondrial function and increased the number of surviving cells after treatment with the cell toxin ionomycin in a dose dependent fashion. Dimebon has also been shown to promote neurite outgrowth and neurogenesis, processes important in the formation of new and/or enhanced neuronal cell connections, and evidence of dimebon's potential for use in additional diseases or conditions. See, e.g., U.S. Pat. Nos. 6,187,785 and 7,071,206 and PCT Patent Application Nos. PCT/US2004/041081, PCT/US2007/020483, PCT/US2006/039077, PCT/US2008/077090, PCT/US2007/020516, PCT/US2007/022645, PCT/US2007/002117, PCT/US2008/006667, PCT/US2007/024626, PCT/US2008/009357, PCT/US2007/024623 and PCT/US2008/008121. All references disclosed herein and throughout, such as publications, patents, patent applications and published patent applications, are incorporated herein by reference in their entireties.

Although dimebon holds great promise as a drug for the treatment of neurodegenerative diseases and/or diseases in which neurite outgrowth and/or neurogenesis may be implicated in therapy, there remains a need for new and alternative therapies for the treatment of such diseases or conditions. In addition, there remains a need for new and alternative antihistamine drugs, preferably ones in which side-effects such as drowsiness are reduced or eliminated. Compounds that exhibit enhanced and/or more desirable properties than dimebon (e.g., superior safety and efficacy) may find particular use in the treatment of at least those indications for which dimebon is believed to be advantageous. Further, compounds that exhibit a different therapeutic profile than dimebon as determined, e.g. by in vitro and/or in vivo assays, may find use in additional diseases and conditions.

BRIEF SUMMARY OF THE INVENTION

Compounds of the general formula (I) are described as new histamine receptor modulators. Other compounds are also detailed herein. Compositions comprising the compounds are provided, as are kits comprising the compound as well as methods of using and making the compounds. Other compounds are also provided. Compounds of the invention may also find use in treating neurodegenerative diseases. Compounds of the invention may also find use in treating diseases and/or conditions in which modulation of aminergic G protein-coupled receptors and/or neurite outgrowth may be implicated in therapy. Compounds disclosed herein may find use in the methods disclosed herein, including use in treating, preventing, delaying the onset and/or delaying the development of a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder and/or a neuronal disorder in an individual in need thereof, such as humans.

The invention embraces compounds of the formula (I):

where:

R¹ is H, hydroxyl, nitro, cyano, halo, substituted or unsubstituted C₁-C₈ alkyl, substituted or unsubstituted C₂-C₈ alkenyl, substituted or unsubstituted C₂-C₈ alkynyl, perhaloalkyl, acyl, acyloxy, carbonylalkoxy, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted aralkyl, C₁-C₈ perhaloalkoxy, alkoxy, aryloxy, carboxyl, thiol, thioalkyl, substituted or unsubstituted amino, acylamino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, aminosulfonyl, sulfonylamino, sulfonyl or carbonylalkylenealkoxy;

each R^(2a) and R^(2b) is independently H, substituted or unsubstituted C₁-C₈ alkyl, halo, cyano, hydroxyl, alkoxy, nitro or R^(2a) and R^(2b) are taken together to form a carbonyl moiety;

each R^(3a) and R^(3b) is independently H, substituted or unsubstituted C₁-C₈ alkyl, halo, cyano or nitro or R^(3a) and R^(3b) are taken together to form a carbonyl moiety;

each X⁷, X⁸, X⁹ and X¹⁰ is independently N or CR⁴;

m and q are independently 0 or 1;

X¹ is N or CH;

each R⁴ is independently H, hydroxyl, nitro, cyano, halo, C₁-C₈ perhaloalkyl, substituted or unsubstituted C₁-C₈ alkyl, substituted or unsubstituted C₂-C₈ alkenyl, substituted or unsubstituted C₂-C₈ alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, C₁-C₈ perhaloalkoxy, C₁-C₈ alkoxy, aryloxy, carboxyl, thiol, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aralkyl, thioalkyl, substituted or unsubstituted amino, acylamino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, aminosulfonyl, sulfonylamino, sulfonyl, carbonylalkylenealkoxy, alkylsulfonylamino or acyl;

each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is independently H, hydroxyl, C₁-C₈ alkyl or is taken together with the carbon to which it is attached and a geminal R^(8(e-f)) to form a cycloalkyl moiety;

each R^(10a) and R^(10b) is independently H, halo, a substituted or unsubstituted C₁-C₈ alkyl, hydroxyl, alkoxyl or R^(10a) and R^(10b) are taken together to form a carbonyl; and

Q is acylamino, carbonylalkoxy, acyloxy, aminoacyl or aminocarbonylalkoxy; provided that: (1) when X is N, the compound is other than a compound in Table 1, and (2) when X¹ is CH, the compound is other than any of 9H-Carbazole-9-acetamide, 5,6,7,8-tetrahydro-3-[[[5-[[(1-methylethyl)sulfonyl]amino]pentyl]amino]carbonyl]-; 9H-Carbazole-9-acetamide, N-ethyl-1,2,3,4-tetrahydro-7-methoxy-2,2-dimethyl-N-2-thiazolyl-; 3,5-Pyridinedicarboxylic acid, 4-(2-chlorophenyl)-2-[[2-[[3-[3-[[(4-fluorophenyl)sulfonyl]amino]-1,2,3,4-tetrahydro-9H-carbazol-9-yl]-1-oxopropyl]amino]ethoxy]methyl]-1,4-dihydro-6-methyl-, 3-methyl5-(1-methylethyl) ester; 9H-Carbazole-9-acetamide, 1,2,3,4-tetrahydro-N-(2-methoxyphenyl)-; 9H-Carbazole-9-acetamide, 1,2,3,4-tetrahydro-7-methoxy-2,2-dimethyl-N,N-bis(3-methylbutyl)-; 3,5-Pyridinedicarboxylic acid, 4-(2,3-dichlorophenyl)-1,4-dihydro-2,6-dimethyl-, 2-[[3-[3-[[(4-fluorophenyl)sulfonyl]amino]-1,2,3,4-tetrahydro-9H-carbazol-9-yl]-1-oxopropyl]amino]ethyl methyl ester; 9H-Carbazole-9-butanamide, N-[4-[(4-aminophenyl)sulfonyl]phenyl]-1,2,3,4-tetrahydro-; Carbamic acid, [(1,2,3,4-tetrahydro-3-methyl-9H-carbazol-9-yl)acetyl]-, ethyl ester; 9H-Carbazole-9-acetamide, 1,2,3,4-tetrahydro-7-methoxy-2,2-dimethyl-N-(2-methylpropyl)-N-propyl-; 9H-Carbazole-9-butanamide, N-(9,10-dihydro-9,10-dioxo-1-anthracenyl)-1,2,3,4-tetrahydro-; 9H-Carbazole-9-acetamide, 1,2,3,4-tetrahydro-7-methoxy-2,2-dimethyl-N,N-dipropyl-; 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-[2-(trifluoromethyl)phenyl]-, 2-[[3-[3-[[(4-fluorophenyl)sulfonyl]amino]-1,2,3,4-tetrahydro-9H-carbazol-9-yl]-1-oxopropyl]amino]ethyl 1-methylethylester; 1H-Carbazole-8-carboxylic acid, 2,3,4,9-tetrahydro-9-[2-[(2-hydroxyethyl)amino]-2-oxoethyl]-; 9H-Carbazole-9-acetamide, N-(cyclopropylmethyl)-1,2,3,4-tetrahydro-7-methoxy-2,2-dimethyl-N-propyl-; 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-, 2-[[3-[3-[[(4-fluorophenyl)sulfonyl]amino]-1,2,3,4-tetrahydro-9H-carbazol-9-yl]-1-oxopropyl]amino]ethyl 1-methylethyl ester; 1H-Carbazole-8-carboxylic acid, 9-[2-(diethylamino)-2-oxoethyl]-2,3,4,9-tetrahydro-; 9H-Carbazole-9-acetamide, N,N-dibutyl-1,2,3,4-tetrahydro-7-methoxy-2,2-dimethyl-; 9H-Carbazole-9-acetamide, 5,6,7,8-tetrahydro-4-methoxy-N,N-dipropyl-; 9H-Carbazole-9-acetamide, N-(3,3-dimethylbutyl)-5,6,7,8-tetrahydro-2-methoxy-5-oxo-N-propyl-; 9H-Carbazole-9-acetamide, N-(2,2-dimethylpropyl)-N-ethyl-5,6,7,8-tetrahydro-2-methoxy-; 9H-Carbazole-9-propanamide, 3-[[(4-chlorophenyl)sulfonyl]amino]-6-fluoro-1,2,3,4-tetrahydro-N,N-dimethyl-; 9H-Carbazole-9-acetamide, N-(3,3-dimethylbutyl)-N-ethyl-5,6,7,8-tetrahydro-2-methoxy-5-oxo-; 9H-Carbazole-9-acetamide, N-(3,3-dimethylbutyl)-N-ethyl-5,6,7,8-tetrahydro-2-methoxy-; Benzamide, N-[1-methyl-3-(1,2,3,4-tetrahydro-9H-carbazol-9-yl)propyl]-3,5-dinitro-; 9H-Carbazole-9-acetamide, N-ethyl-5,6,7,8-tetrahydro-2-methoxy-N-(3-methylbutyl)-5-oxo-; 9H-Carbazole-9-acetamide, N-butyl-N-ethyl-5,6,7,8-tetrahydro-2-methoxy-; 9H-Carbazole-9-acetamide, 1,2,3,4-tetrahydro-1-hydroxy-; 9H-Carbazole-9-acetamide, N-ethyl-5,6,7,8-tetrahydro-2-methoxy-N-(2-methylpropyl)-5-oxo-; 9H-Carbazole-9-acetamide, N-(cyclopropylmethyl)-5,6,7,8-tetrahydro-2-methoxy-N-propyl-; Acetamide, N-[3-(1,2,3,4-tetrahydro-1-oxo-9H-carbazol-9-yl)propyl]-; 9H-Carbazole-9-acetamide, N-cyclohexyl-N-ethyl-5,6,7,8-tetrahydro-2-methoxy-5-oxo-; 9H-Carbazole-9-acetamide, N-ethyl-5,6,7,8-tetrahydro-2-methoxy-N-(3-methylbutyl)-; Carbamic acid, [(1S)-2-(6-chloro-1,2,3,4-tetrahydro-9H-carbazol-9-yl)-1-methylethyl]-, 1,1-dimethylethyl ester; 9H-Carbazole-9-acetamide, 5,6,7,8-tetrahydro-2-methoxy-N,N-bis(2-methylpropyl)-5-oxo-; 3,5-Pyridinedicarboxylic acid, 4-(2-chlorophenyl)-2-[[2-[[3-[3-[[(4-fluorophenyl)sulfonyl]amino]-1,2,3,4-tetrahydro-9H-carbazol-9-yl]-1-oxopropyl]amino]ethoxy]methyl]-1,4-dihydro-6-methyl-, 3-ethyl5-(1-methylethyl) ester; 9H-Carbazole-9-acetamide, 5,6,7,8-tetrahydro-2-methoxy-N,N-dipropyl-; Benzamide, 3,5-dinitro-N-[3-(1,2,3,4-tetrahydro-9H-carbazol-9-yl)propyl]-; Carbamic acid, [(1S)-2-(7-chloro-1,2,3,4-tetrahydro-9H-carbazol-9-yl)-1-methylethyl]-, 1,1-dimethylethyl ester; 9H-Carbazole-9-acetamide, N-(3,3-dimethylbutyl)-1,2,3,4-tetrahydro-7-methoxy-2,2-dimethyl-N-propyl-; 3,5-Pyridinedicarboxylic acid, 2-[[2-[[3-[3-[[(4-fluorophenyl)sulfonyl]amino]-1,2,3,4-tetrahydro-9H-carbazol-9-yl]-1-oxopropyl]amino]ethoxy]methyl]-1,4-dihydro-6-methyl-4-[2-(phenylmethoxy)phenyl]-, 3-ethyl 5-methyl ester; 9H-Carbazole-9-acetamide, N-(4-ethoxyphenyl)-1,2,3,4-tetrahydro-; 9H-Carbazole-9-acetamide, 1,2,3,4-tetrahydro-6-methyl-1-oxo-; 9H-Carbazole-9-acetamide, N-(3,3-dimethylbutyl)-N-ethyl-1,2,3,4-tetrahydro-7-methoxy-2,2-dimethyl-; 9H-Carbazole-9-propanamide, 3-[[(4-fluorophenyl)sulfonyl]amino]-1,2,3,4-tetrahydro-N-(2-hydroxyethyl)-, (R)—; Glycine, N-[(1,2,3,4-tetrahydro-3-methyl-9H-carbazol-9-yl)acetyl]-, ethyl ester; 9H-Carbazole-9-acetamide, N-ethyl-1,2,3,4-tetrahydro-7-methoxy-2,2-dimethyl-N-(3-methylbutyl)-; 3,5-Pyridinedicarboxylic acid, 4-(2-chlorophenyl)-1,4-dihydro-2,6-dimethyl-, 2-[[3-[3-[[(4-fluorophenyl)sulfonyl]amino]-1,2,3,4-tetrahydro-9H-carbazol-9-yl]-1-oxopropyl]amino]ethyl methyl ester; 9H-Carbazole-9-butanamide, N-(2-benzoyl-4-chlorophenyl)-1,2,3,4-tetrahydro-; 9H-Carbazole-9-acetamide, N-ethyl-1,2,3,4-tetrahydro-7-methoxy-2,2-dimethyl-N-(2-methylpropyl)-; 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-, 2-[[3-[3-[[(4-fluorophenyl)sulfonyl]amino]-1,2,3,4-tetrahydro-9H-carbazol-9-yl]-1-oxopropyl]amino]ethyl methyl ester; 9H-Carbazole-9-butanamide, N-(9,10-dihydro-9,10-dioxo-2-anthracenyl)-1,2,3,4-tetrahydro-; 9H-Carbazole-9-acetamide, N-cyclohexyl-N-ethyl-1,2,3,4-tetrahydro-7-methoxy-2,2-dimethyl-; 3,5-Pyridinedicarboxylic acid, 4-(3-chlorophenyl)-1,4-dihydro-2,6-dimethyl-, 2-[[3-[3-[[(4-fluorophenyl)sulfonyl]amino]-1,2,3,4-tetrahydro-9H-carbazol-9-yl]-1-oxopropyl]amino]ethyl 1-methylethyl ester; 1H-Carbazole-8-carboxylic acid, 9-(2-amino-2-oxoethyl)-2,3,4,9-tetrahydro-; 9H-Carbazole-9-propanamide, 1,2,3,4-tetrahydro-6-methyl-1-oxo-; 9H-Carbazole-9-acetamide, 1,2,3,4-tetrahydro-7-methoxy-2,2-dimethyl-N,N-bis(2-methylpropyl)-; 9H-Carbazole-9-propanamide, 3-[[(4-fluorophenyl)sulfonyl]amino]-1,2,3,4-tetrahydro-; 1H-Carbazole-8-carboxylic acid, 9-[2-(dimethylamino)-2-oxoethyl]-2,3,4,9-tetrahydro-; 9H-Carbazole-9-acetamide, N-ethyl-5,6,7,8-tetrahydro-4-methoxy-N-(3-methylbutyl)-; 9H-Carbazole-9-propanamide, 3-[[(4-fluorophenyl)sulfonyl]amino]-1,2,3,4-tetrahydro-N-(methylsulfonyl)-, (R)—; 9H-Carbazole-9-acetamide, N,N-dibutyl-5,6,7,8-tetrahydro-4-methoxy-; 9H-Carbazole-9-propanamide, 3-[[(4-chlorophenyl)sulfonyl]amino]-6-fluoro-1,2,3,4-tetrahydro-; 9H-Carbazole-9-acetamide, N-ethyl-5,6,7,8-tetrahydro-2-methoxy-5-oxo-N-2-thiazolyl-; 9H-Carbazole-9-acetamide, N-ethyl-5,6,7,8-tetrahydro-2-methoxy-N-2-thiazolyl-; 9H-Carbazole-9-propanamide, 1,2,3,4-tetrahydro-1-oxo-; 9H-Carbazole-9-acetamide, 5,6,7,8-tetrahydro-2-methoxy-N,N-bis(3-methylbutyl)-5-oxo-; 9H-Carbazole-9-acetamide, N-butyl-5,6,7,8-tetrahydro-2-methoxy-N-propyl-; 9H-Carbazole-9-acetamide, 5,6,7,8-tetrahydro-2-methoxy-N-(2-methylpropyl)-5-oxo-N-propyl-; 9H-Carbazole-9-acetamide, N-cyclohexyl-N-ethyl-5,6,7,8-tetrahydro-2-methoxy-; 9H-Carbazole-9-acetamide, 1,2,3,4-tetrahydro-1-oxo-; 9H-Carbazole-9-acetamide, 5,6,7,8-tetrahydro-2-methoxy-5-oxo-N,N-dipropyl-; 9H-Carbazole-9-acetamide, 5,6,7,8-tetrahydro-2-methoxy-N,N-bis(2-methylpropyl)-; Acetamide, N-[2-(1,2,3,4-tetrahydro-1-oxo-9H-carbazol-9-yl)ethyl]-; 9H-Carbazole-9-acetamide, N-(cyclopropylmethyl)-5,6,7,8-tetrahydro-2-methoxy-5-oxo-N-propyl-; 3,5-Pyridinedicarboxylic acid, 4-(2,1,3-benzoxadiazol-4-yl)-2-[[2-[[3-[3-[[(4-fluorophenyl)sulfonyl]amino]-1,2,3,4-tetrahydro-9H-carbazol-9-yl]-1-oxopropyl]amino]ethoxy]methyl]-1,4-dihydro-6-methyl-, 3-ethyl5-(1-methylethyl) ester; 9H-Carbazole-9-acetamide, 5,6,7,8-tetrahydro-2-methoxy-N,N-bis(3-methylbutyl)-; Carbamic acid, [(1S)-2-(7-bromo-1,2,3,4-tetrahydro-9H-carbazol-9-yl)-1-methylethyl]-, 1,1-dimethylethyl ester; 9H-Carbazole-9-acetamide, N,N-dibutyl-5,6,7,8-tetrahydro-2-methoxy-5-oxo-; 3,5-Pyridinedicarboxylic acid, 2-[[2-[[3-[3-[[(4-fluorophenyl)sulfonyl]amino]-1,2,3,4-tetrahydro-9H-carbazol-9-yl]-1-oxopropyl]amino]ethoxy]methyl]-1,4-dihydro-6-methyl-4-(3-nitrophenyl)-, 3-ethyl 5-methyl ester; 9H-Carbazole-9-acetamide, N,N-dibutyl-5,6,7,8-tetrahydro-2-methoxy-; Carbazole-9-acetanilide, 1,2,3,4-tetrahydro-6-methyl-1-oxo-; and 3,5-Pyridinedicarboxylic acid, 4-(3-chlorophenyl)-1,4-dihydro-2,6-dimethyl-, 2-[[3-[3-[[(4-fluorophenyl)sulfonyl]amino]-1,2,3,4-tetrahydro-9H-carbazol-9-yl]-1-oxopropyl]amino]ethyl methyl ester.

TABLE 1 Compound No. Compound Name  1x 2H-Pyrido[4,3-b]indole-2-carboxylic acid, 5-[2-(dimethylamino)-2-oxoethyl]- 1,3,4,5-tetrahydro-8-[(4-methyl-1-piperidinyl)carbonyl]-, 1,1-dimethylethyl ester  2x 5H-Pyrido[4,3-b]indole-5-acetamide, 1,2,3,4-tetrahydro-N,N-dimethyl-8-[(4- methyl-1-piperidinyl)carbonyl]-  3x 5H-Pyrido[4,3-b]indole-5-acetamide, 2-cyclobutyl-1,2,3,4-tetrahydro-N,N- dimethyl-8-[(4-methyl-1-piperidinyl)carbonyl]-  4x 5H-Pyrido[4,3-b]indole-5-acetamide, 2-cyclohexyl-1,2,3,4-tetrahydro-N,N- dimethyl-8-[(4-methyl-1-piperidinyl)carbonyl]-  5x 5H-Pyrido[4,3-b]indole-5-acetamide, 2-cyclopentyl-1,2,3,4-tetrahydro-N,N- dimethyl-8-[(4-methyl-1-piperidinyl)carbonyl]-  6x 5H-Pyrido[4,3-b]indole-5-acetamide, 8-formyl-1,2,3,4-tetrahydro-2-(1- methylethyl)-  7x 1H-Pyrido[4,3-b]indole-2,5-dipropanoic acid, 3,4-dihydro-8-methyl-, 2,5- diethyl ester  8x 1H-Pyrido[4,3-b]indole-2-butanoic acid, 5-(2-ethoxy-2-oxoethyl)-8-fluoro- 3,4-dihydro-, ethyl ester  9x 1H-Pyrido[4,3-b]indole-2-propanoic acid, 5-(2-ethoxy-2-oxoethyl)-8-fluoro- 3,4-dihydro-, ethyl ester 10x 2H-Pyrido[4,3-b]indole-2-butanoic acid, 5-(3-ethoxy-3-oxopropyl)-1,3,4,5- tetrahydro-8-methyl-, ethyl ester 11x 5H-Pyrido[4,3-b]indole-5-acetamide, 1,2,3,4-tetrahydro-2-(1-methylethyl)- 12x 5H-Pyrido[4,3-b]indole-5-acetamide, 1,2,3,4-tetrahydro-2,8-bis(1- methylethyl)- 13x 5H-Pyrido[4,3-b]indole-5-acetamide, 1,2,3,4-tetrahydro-8-methyl-2-(1- methylethyl)- 14x 5H-Pyrido[4,3-b]indole-5-acetamide, N-cyclohexyl-1,2,3,4-tetrahydro-2-(1- methylethyl)- 15x 5H-Pyrido[4,3-b]indole-5-acetamide, N-cyclopentyl-1,2,3,4-tetrahydro-2-(1- methylethyl)- 16x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-, ethyl ester 17x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-2-(1- naphthalenylcarbonyl)-, ethyl ester 18x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-2-(2-phenylethyl)-, ethyl ester 19x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-2-(4- pyridinylmethyl)-, ethyl ester 20x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-2,8-dimethyl-, ethyl ester 21x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-2- [(phenylamino)carbonyl]-, ethyl ester 22x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-2- [(phenylmethoxy)carbonyl]-, ethyl ester 23x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-2-[2-(3- pyridinyl)ethyl]-, ethyl ester 24x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-2-methyl-, ethyl ester 25x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-2-methyl-6- (trifluoromethyl)-, ethyl ester 26x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-2-methyl-8- (trifluoromethyl)-, ethyl ester 27x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-6-(trifluoromethyl)-, ethyl ester 28x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-7-methyl-, ethyl ester 29x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-8-(trifluoromethyl)-, ethyl ester 30x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-8-[(4-methyl-1- piperidinyl)carbonyl]-, ethyl ester 31x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-8-methyl-, ethyl ester 32x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-8-methyl-2-(4- pyridinylmethyl)-, ethyl ester 33x 5H-Pyrido[4,3-b]indole-5-acetic acid, 1,2,3,4-tetrahydro-8-methyl-2-[2-(3- pyridinyl)ethyl]-, ethyl ester 34x 5H-Pyrido[4,3-b]indole-5-acetic acid, 2-(2-cyclohexyl-2-phenylacetyl)- 1,2,3,4-tetrahydro-, ethyl ester 35x 5H-Pyrido[4,3-b]indole-5-acetic acid, 2-(ethoxycarbonyl)-1,2,3,4-tetrahydro-, methyl ester 36x 5H-Pyrido[4,3-b]indole-5-acetic acid, 2-[(1,1-dimethylethoxy)carbonyl]- 1,2,3,4-tetrahydro-, ethyl ester 37x 5H-Pyrido[4,3-b]indole-5-acetic acid, 2-[(1,1-dimethylethoxy)carbonyl]- 1,2,3,4-tetrahydro-, methyl ester 38x 5H-Pyrido[4,3-b]indole-5-acetic acid, 2-[(1,1-dimethylethoxy)carbonyl]- 1,2,3,4-tetrahydro-6-(trifluoromethyl)-, ethyl ester 39x 5H-Pyrido[4,3-b]indole-5-acetic acid, 2-[(1,1-dimethylethoxy)carbonyl]- 1,2,3,4-tetrahydro-8-(trifluoromethyl)-, ethyl ester 40x 5H-Pyrido[4,3-b]indole-5-acetic acid, 2-[(1,1-dimethylethoxy)carbonyl]- 1,2,3,4-tetrahydro-8-[(4-methyl-1-piperidinyl)carbonyl]-, ethyl ester 41x 5H-Pyrido[4,3-b]indole-5-acetic acid, 2-[(1,1-dimethylethoxy)carbonyl]- 1,2,3,4-tetrahydro-8-methyl-, ethyl ester 42x 5H-Pyrido[4,3-b]indole-5-acetic acid, 2-[(1,1-dimethylethoxy)carbonyl]-6- fluoro-1,2,3,4-tetrahydro-, ethyl ester 43x 5H-Pyrido[4,3-b]indole-5-acetic acid, 2-[(1,1-dimethylethoxy)carbonyl]-8- fluoro-1,2,3,4-tetrahydro-, ethyl ester 44x 5H-Pyrido[4,3-b]indole-5-acetic acid, 2-[(2-ethoxy-1-naphthalenyl)carbonyl]- 1,2,3,4-tetrahydro-, ethyl ester 45x 5H-Pyrido[4,3-b]indole-5-acetic acid, 2-benzoyl-1,2,3,4-tetrahydro-8- methoxy-, ethyl ester 46x 5H-Pyrido[4,3-b]indole-5-acetic acid, 2-cyclobutyl-1,2,3,4-tetrahydro-8-[(4- methyl-1-piperidinyl)carbonyl]-, methyl ester 47x 5H-Pyrido[4,3-b]indole-5-acetic acid, 2-cyclohexyl-1,2,3,4-tetrahydro-8-[(4- methyl-1-piperidinyl)carbonyl]-, methyl ester 48x 5H-Pyrido[4,3-b]indole-5-acetic acid, 2-cyclopentyl-1,2,3,4-tetrahydro-8-[(4- methyl-1-piperidinyl)carbonyl]-, methyl ester 49x 5H-Pyrido[4,3-b]indole-5-acetic acid, 6-chloro-1,2,3,4-tetrahydro-, ethyl ester 50x 5H-Pyrido[4,3-b]indole-5-acetic acid, 6-fluoro-1,2,3,4-tetrahydro-, ethyl ester 51x 5H-Pyrido[4,3-b]indole-5-acetic acid, 6-fluoro-1,2,3,4-tetrahydro-2-methyl-, ethyl ester 52x 5H-Pyrido[4,3-b]indole-5-acetic acid, 7-chloro-1,2,3,4-tetrahydro-, ethyl ester 53x 5H-Pyrido[4,3-b]indole-5-acetic acid, 8-bromo-1,2,3,4-tetrahydro-, ethyl ester 54x 5H-Pyrido[4,3-b]indole-5-acetic acid, 8-chloro-1,2,3,4-tetrahydro-, ethyl ester 55x 5H-Pyrido[4,3-b]indole-5-acetic acid, 8-fluoro-1,2,3,4-tetrahydro-, ethyl ester 56x 5H-Pyrido[4,3-b]indole-5-acetic acid, 8-fluoro-1,2,3,4-tetrahydro-2-(2- phenylethyl)-, ethyl ester 57x 5H-Pyrido[4,3-b]indole-5-acetic acid, 8-fluoro-1,2,3,4-tetrahydro-2-(3- pyridinylmethyl)-, ethyl ester 58x 5H-Pyrido[4,3-b]indole-5-acetic acid, 8-fluoro-1,2,3,4-tetrahydro-2-(4- pyridinylmethyl)-, ethyl ester 59x 5H-Pyrido[4,3-b]indole-5-acetic acid, 8-fluoro-1,2,3,4-tetrahydro-2- (phenylmethyl)-, ethyl ester 60x 5H-Pyrido[4,3-b]indole-5-acetic acid, 8-fluoro-1,2,3,4-tetrahydro-2-[2-(3- pyridinyl)ethyl]-, ethyl ester 61x 5H-Pyrido[4,3-b]indole-5-acetic acid, 8-fluoro-1,2,3,4-tetrahydro-2-[2-(4- pyridinyl)ethyl]-, ethyl ester 62x 5H-Pyrido[4,3-b]indole-5-acetic acid, 8-fluoro-1,2,3,4-tetrahydro-2-methyl-, ethyl ester 63x 5H-Pyrido[4,3-b]indole-5-propanamide,1,2,3,4-tetrahydro-2-methyl- 64x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-, ethyl ester 65x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-1,1,3,3- tetramethyl-, 2-(diethylamino)ethyl ester 66x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-1,1,3,3- tetramethyl-, 2-(dimethylamino)ethyl ester 67x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-1,1,3,3- tetramethyl-, ethyl ester 68x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-2-(2- phenylethyl)-6-(trifluoromethyl)-, ethyl ester 69x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-2-(3- pyridinylmethyl)-, ethyl ester 70x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-2-(4- pyridinylmethyl)-8-(trifluoromethyl)-, ethyl ester 71x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-2- (phenylmethyl)-6-(trifluoromethyl)-, ethyl ester 72x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-2- (phenylsulfonyl)-, ethyl ester 73x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-2,8-dimethyl-, ethyl ester 74x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-2-[2-(3- pyridinyl)ethyl]-, ethyl ester 75x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-2-[2-(3- pyridinyl)ethyl]-8-(trifluoromethyl)-, ethyl ester 76x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-2-methyl-, ethyl ester 77x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-2-methyl-6- (trifluoromethyl)-, ethyl ester 78x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-2-methyl-8- (trifluoromethyl)-, ethyl ester 79x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-6- (trifluoromethyl)-, ethyl ester 80x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-8- (trifluoromethyl)-, ethyl ester 81x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-8-methyl-, ethyl ester 82x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 1,2,3,4-tetrahydro-8-methyl-2- (phenylsulfonyl)-, ethyl ester 83x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 2-(ethoxycarbonyl)-1,2,3,4- tetrahydro-6-(trifluoromethyl)-, ethyl ester 84x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 2-(ethoxycarbonyl)-1,2,3,4- tetrahydro-8-(trifluoromethyl)-, ethyl ester 85x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 2-(ethoxycarbonyl)-6-fluoro- 1,2,3,4-tetrahydro-, ethyl ester 86x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 2-[(1,1-dimethylethoxy)carbonyl]- 1,2,3,4-tetrahydro-, ethyl ester 87x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 2-[(1,1-dimethylethoxy)carbonyl]- 1,2,3,4-tetrahydro-8-methyl-, ethyl ester 88x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 2-[(1,1-dimethylethoxy)carbonyl]- 8-fluoro-1,2,3,4-tetrahydro-, ethyl ester 89x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 2-[(3,4-dimethylphenyl)methyl]-8- fluoro-1,2,3,4-tetrahydro-, ethyl ester 90x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 2-[(4-chlorophenyl)methyl]-8- fluoro-1,2,3,4-tetrahydro-, ethyl ester 91x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 2-[(4-fluorophenyl)sulfonyl]- 1,2,3,4-tetrahydro-, ethyl ester 92x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 2-[(4-fluorophenyl)sulfonyl]- 1,2,3,4-tetrahydro-8-methyl-, ethyl ester 93x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 6-fluoro-1,2,3,4-tetrahydro-, ethyl ester 94x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 6-fluoro-1,2,3,4-tetrahydro-2-[2-(4- pyridinyl)ethyl]-, ethyl ester 95x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 6-fluoro-1,2,3,4-tetrahydro-2- methyl-, ethyl ester 96x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 8-(ethoxycarbonyl)-1,2,3,4- tetrahydro-1,1,3,3-tetramethyl-, ethyl ester 97x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 8-fluoro-1,2,3,4-tetrahydro-, ethyl ester 98x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 8-fluoro-1,2,3,4-tetrahydro-2-(2- thienylmethyl)-, ethyl ester 99x 5H-Pyrido[4,3-b]indole-5-propanoic acid, 8-fluoro-1,2,3,4-tetrahydro-2-(3- pyridinylmethyl)-, ethyl ester 100x  5H-Pyrido[4,3-b]indole-5-propanoic acid, 8-fluoro-1,2,3,4-tetrahydro-2-(4- pyridinylmethyl)-, ethyl ester 101x  5H-Pyrido[4,3-b]indole-5-propanoic acid, 8-fluoro-1,2,3,4-tetrahydro-2- (phenylmethyl)-, ethyl ester 102x  5H-Pyrido[4,3-b]indole-5-propanoic acid, 8-fluoro-1,2,3,4-tetrahydro-2- (phenylsulfonyl)-, ethyl ester 103x  5H-Pyrido[4,3-b]indole-5-propanoic acid, 8-fluoro-1,2,3,4-tetrahydro-2-[2-(3- pyridinyl)ethyl]-, ethyl ester 104x  5H-Pyrido[4,3-b]indole-5-propanoic acid, 8-fluoro-1,2,3,4-tetrahydro-2- methyl-, ethyl ester 105x  5H-Pyrido[4,3-b]indole-5-propanoic acid, 8-fluoro-2-(2-furanylmethyl)- 1,2,3,4-tetrahydro-, ethyl ester 106x  5H-Pyrido[4,3-b]indole-5-propanoic acid, 8-fluoro-2-[(4- fluorophenyl)sulfonyl]-1,2,3,4-tetrahydro-, ethyl ester 107x  5H-Pyrrolo[2,3-c:4,5-c′]dipyridine-5-acetamide, 1,2,3,4-tetrahydro-2-(1- methylethyl)- 108x  5H-Pyrrolo[2,3-c:4,5-c′]dipyridine-5-acetamide, N-cyclohexyl-1,2,3,4- tetrahydro-2-(1-methylethyl)- 109x  5H-Pyrrolo[3,2-c:4,5-c′]dipyridine-5-acetamide, 1,2,3,4-tetrahydro-2-(1- methylethyl)- 110x  5H-Pyrrolo[3,2-c:4,5-c′]dipyridine-5-acetamide, N-cyclohexyl-1,2,3,4- tetrahydro-2-(1-methylethyl)-

The listing under proviso (1) above is also referred to herein as “proviso 1.” The listing under proviso (2) above is also referred to herein as “proviso 2.”

In one variation, the compound is of the formula (I) wherein the compound further is a type 1 compound. In another variation, the compound is of the formula (I) wherein the compound further is a type 2 compound. In yet another variation, the compound is of the formula (I) wherein the compound further is a type 3 compound. In a further variation, the compound is of the formula (I) wherein the compound further is a type 4 compound.

Other compounds are also detailed herein, including but not limited to compounds of the Formula (E):

wherein:

R¹ is H, hydroxyl, nitro, cyano, halo, substituted or unsubstituted C₁-C₈ alkyl, substituted or unsubstituted C₂-C₈ alkenyl, substituted or unsubstituted C₂-C₈ alkynyl, perhaloalkyl, acyl, acyloxy, carbonylalkoxy, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted aralkyl, C₁-C₈ perhaloalkoxy, alkoxy, aryloxy, carboxyl, thiol, thioalkyl, substituted or unsubstituted amino, acylamino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, aminosulfonyl, sulfonylamino, sulfonyl or carbonylalkylenealkoxy;

each R^(2a) and R^(2b) is independently H, substituted or unsubstituted C₁-C₈ alkyl, halo, cyano, hydroxyl, alkoxy, nitro or R^(2a) and R^(2b) are taken together with the carbon to which they are attached to form a cycloalkyl moiety or a carbonyl moiety;

each R^(3a) and R^(3b) is independently H, substituted or unsubstituted C₁-C₈ alkyl, halo, cyano hydroxyl, alkoxy, nitro or R^(3a) and R^(3b) are taken together with the carbon to which they are attached to form a cycloalkyl moiety or a carbonyl moiety;

each X⁷, X⁸, X⁹ and X¹⁰ is independently N or CR⁴;

m and q are independently 0 or 1;

n is 0 or 1;

each R⁴ is independently H, hydroxyl, nitro, cyano, halo, C₁-C₈ perhaloalkyl, substituted or unsubstituted C₁-C₈ alkyl, substituted or unsubstituted C₂-C₈ alkenyl, substituted or unsubstituted C₂-C₈ alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, C₁-C₈ perhaloalkoxy, C₁-C₈ alkoxy, aryloxy, carboxyl, thiol, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aralkyl, thioalkyl, substituted or unsubstituted amino, acylamino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, aminosulfonyl, sulfonylamino, sulfonyl, carbonylalkylenealkoxy, alkylsulfonylamino or acyl;

each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is independently H, hydroxyl, substituted or unsubstituted alkyl or is taken together with the carbon to which it is attached and a geminal R^(8(a-f)) to form a cycloalkyl moiety;

each R^(10a) and R^(10b) is independently H, substituted or unsubstituted C₁-C₈ alkyl, halo, hydroxyl, alkoxyl or R^(10a) and R^(10b) are taken together with the carbon to which they are attached to form a cycloalkyl moiety or a carbonyl moiety; and

Q is acyclic or cyclic acylamino, carbonylalkoxy, acyloxy, aminoacyl, aminocarbonylalkoxy, substituted or unsubstituted lactam or substituted or unsubstituted cycloalkyl;

provided that: (ia) Q is substituted or unsubstituted cycloalkyl or a lactam moiety when each of m, n and q is 0 and (ib) m, n and q are 0 when Q is a substituted or unsubstituted cycloalkyl or a lactam moiety, (ii) Q is cyclic acylamino only when each of m, n and q is 1, (iii) when Q is carbonylalkoxy, each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is other than cycloalkyl and substituted alkyl; (iv) the compound is other than a compound in Table 1, and (v) the compound is other than 5-cyclohexyl-2,3,4,5-tetrahydro-2-methyl-1H-pyrido[4,3-b]indole and 5-cyclopentyl-2,3,4,5-tetrahydro-2-[(4-methyl-1H-imidazol-5-yl)methyl]-1H-pyrido[4,3-b]indol-1-one;.

or a salt thereof.

Compounds of the formula (Vc) are also detailed herein:

wherein: R¹ is methyl; m and q are independently 0 or 1; each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is independently H, hydroxyl, substituted or unsubstituted alkyl or is taken together with the carbon to which it is attached and a geminal R^(8(a-f)) to form a cycloalkyl moiety; and Q is acyclic or cyclic acylamino, carbonylalkoxy, acyloxy, aminoacyl or aminocarbonylalkoxy, or a salt thereof.

Compounds of the formula (Vf) are also detailed herein:

wherein: R¹ is methyl; R⁴ is chloro or methyl; m and q are independently 0 or 1; each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is independently H, hydroxyl, substituted or unsubstituted alkyl or is taken together with the carbon to which it is attached and a geminal R^(8(a-f)) to form a cycloalkyl moiety; and Q is acyclic or cyclic acylamino, carbonylalkoxy, acyloxy, aminoacyl or aminocarbonylalkoxy; provided that when R⁴ is methyl, Q is acyclic or cyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy, or a salt thereof.

The invention also includes all salts of compounds referred to herein, such as pharmaceutically acceptable salts. The invention also includes any or all of the stereochemical forms, including any enantiomeric or diastereomeric forms, and any tautomers or other forms of the compounds described. Unless stereochemistry is explicitly indicated in a chemical structure or name, the structure or name is intended to embrace all possible stereoisomers of a compound depicted. In addition, where a specific stereochemical form is depicted, it is understood that other stereochemical forms are also embraced by the invention. All forms of the compounds are also embraced by the invention, such as crystalline or non-crystalline forms of the compounds. Compositions comprising a compound of the invention are also intended, such as a composition of substantially pure compound, including a specific stereochemical form thereof. Compositions comprising a mixture of compounds of the invention in any ratio are also embraced by the invention, including mixtures of two or more stereochemical forms of a compound of the invention in any ratio, such that racemic, non-racemic, enantioenriched and scalemic mixtures of a compound are embraced.

In one aspect, compounds of the invention are used to treat, prevent, delay the onset and/or delay the development of any one or more of the following: cognitive disorders, psychotic disorders, neurotransmitter-mediated disorders and/or neuronal disorders in individuals in need thereof, such as humans. In one variation, compounds of the invention are used to treat, prevent, delay the onset and/or delay the development of diseases or conditions for which the modulation of an aminergic G protein-coupled receptor is believed to be or is beneficial. In one variation, compounds of the invention are used to treat, prevent, delay the onset and/or delay the development of any one or more of diseases or conditions for which neurite outgrowth and/or neurogenesis and/or neurotrophic effects are believed to be or are beneficial. In another variation, compounds of the invention are used to treat, prevent, delay the onset and/or delay the development of diseases or conditions for which the modulation of an aminergic G protein-coupled receptor and neurite outgrowth and/or neurogenesis and/or neurotrophic effects are believed to be or are beneficial. In one variation, the disease or condition is a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder and/or a neuronal disorder.

In another aspect, compounds of the invention are used to improve cognitive function and/or reduce psychotic effects in an individual, comprising administering to an individual in need thereof an amount of a compound described herein or a pharmaceutically acceptable salt thereof effective to improve cognitive function and/or reduce psychotic effects.

In a further aspect, compounds of the invention are used to stimulate neurite outgrowth and/or promote neurogenesis and/or enhance neurotrophic effects in an individual comprising administering to an individual in need thereof an amount of a compound described herein or a pharmaceutically acceptable salt thereof effective to stimulate neurite outgrowth and/or to promote neurogenesis and/or to enhance neurotrophic effects. Synapse loss is associated with a variety of neurodegenerative diseases and conditions including Alzheimer's disease, Huntington's disease, stroke, head trauma and spinal cord injury. Compounds of the invention that stimulate neurite outgrowth may have a benefit in these settings.

In another aspect, compounds described herein are used to modulate an aminergic G protein-coupled receptor comprising administering to an individual in need thereof an amount of a compound described herein or a pharmaceutically acceptable salt thereof effective to modulate an aminergic G protein-coupled receptor. In one variation, a compound of the invention modulates at least one of the following receptors: adrenergic receptor (e.g., α1D, α2A and/or α2B), serotonin receptor (e.g., 5-HT2A, 5-HT2C, 5-HT6 and/or 5-HT7), dopamine receptor (e.g., D2L) and histamine receptor (e.g., H1, H2 and/or H3). In another variation, at least two of the following receptors are modulated: adrenergic receptor (e.g., α1D, α2A and/or α2B), serotonin receptor (e.g., 5-HT2A, 5-HT2C, 5-HT6 and/or 5-HT7), dopamine receptor (e.g., D2L) and histamine receptor (e.g., H1, H2 and/or H3). In another variation, at least three of the following receptors are modulated: adrenergic receptor (e.g., α1D, α2A and/or α2B), serotonin receptor (e.g., 5-HT2A, 5-HT2C, 5-HT6 and/or 5-HT7), dopamine receptor (e.g., D2L) and histamine receptor (e.g., H1, H2 and/or H3). In another variation, each of the following receptors is modulated: adrenergic receptor (e.g., α1D, α2A and/or α2B), serotonin receptor (e.g., 5-HT2A, 5-HT2C, 5-HT6 and/or 5-HT7), dopamine receptor (e.g., D2L) and histamine receptor (e.g., H1, H2 and/or H3). In another variation, at least one of the following receptors is modulated: α1D, α2A, α2B, 5-HT2A, 5-HT2C, 5-HT6,5-HT7, D2L, H1, H2 and H3. In another variation, at least two or three or four or five or six or seven or eight or nine or ten or eleven of the following receptors are modulated: α1D, α2A, α2B, 5-HT2A, 5-HT2C, 5-HT6,5-HT7, D2L, H1, H2 and H3. In a particular variation, at least dopamine receptor D2L is modulated. In another particular variation, at least dopamine receptor D2L and serotonin receptor 5-HT2A are modulated. In a further particular variation, at least adrenergic receptors α1D, α2A, α2B and serotonin receptor 5-HT6 are modulated. In another particular variation, at least adrenergic receptors α1D, α2A, α2B, serotonin receptor 5-HT6 and one or more of serotonin receptor 5-HT7,5-HT2A, 5-HT2C and histamine receptor H1 and H2 are modulated. In a further particular variation, histamine receptor H1 is modulated. In another variation, compounds of the invention exhibit any receptor modulation activity detailed herein and further stimulate neurite outgrowth and/or neurogenesis and/or enhance neurotrophic effects.

The invention is also directed to pharmaceutical compositions comprising a compound of the invention and a pharmaceutically acceptable carrier or excipient. Kits comprising a compound of the invention and instructions for use are also embraced by this invention.

DETAILED DESCRIPTION OF THE INVENTION Definitions

For use herein, unless clearly indicated otherwise, use of the terms “a”, “an” and the like refers to one or more.

The term “about” as used herein refers to the usual range of variation for the respective value readily known to the skilled person in this technical field. Reference to “about” a value or parameter herein includes (and describes) embodiments that are directed to that value or parameter per se.

As used herein, the term “aminergic G protein-coupled receptors” refers to a family of transmembrane proteins involved in cellular communication. Aminergic G protein coupled receptors are activated by biogenic amines and represent a subclass of the superfamily of G protein coupled receptors, which are structurally characterized by seven transmembrane helices. Aminergic G protein-coupled receptors include but are not limited to adrenergic receptors, serotonin receptors, dopamine receptors, histamine receptors and imidazoline receptors.

As used herein, the term “adrenergic receptor modulator” intends and encompasses a compound that binds to or inhibits binding of a ligand to an adrenergic receptor or reduces or eliminates or increases or enhances or mimics an activity of an adrenergic receptor. As such, an “adrenergic receptor modulator” encompasses both an adrenergic receptor antagonist and an adrenergic receptor agonist. In some aspects, the adrenergic receptor modulator binds to or inhibits binding to a ligand to an α1-adrenergic receptor (e.g., α1A, α1B and/or α1D) and/or a α2-adrenergic receptor (e.g., α2A, α2B and/or α2C) and/or reduces or eliminates or increases or enhances or mimics an activity of a α1-adrenergic receptor (e.g., α1A, α1B and/or α1D) and/or a α2-adrenergic receptor (e.g., α2A, α2B and/or α2C) in a reversible or irreversible manner. In some aspects, the adrenergic receptor modulator inhibits binding of a ligand by at least about or about any one of 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 100% as determined in the assays described herein. In some aspects, the adrenergic receptor modulator reduces an activity of an adrenergic receptor by at least or about any of 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 100% as compared to the corresponding activity in the same subject prior to treatment with the adrenergic receptor modulator or compared to the corresponding activity in other subjects not receiving the adrenergic receptor modulator. In some aspects, the adrenergic receptor modulator enhances an activity of an adrenergic receptor by at least about or about any of 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 100 or 200% or 300% or 400% or 500% or more as compared to the corresponding activity in the same subject prior to treatment with the adrenergic receptor modulator or compared to the corresponding activity in other subjects not receiving the adrenergic receptor modulator. In some aspects, the adrenergic receptor modulator is capable of binding to the active site of an adrenergic receptor (e.g., a binding site for a ligand). In some embodiments, the adrenergic receptor modulator is capable of binding to an allosteric site of an adrenergic receptor.

As used herein, the term “dopamine receptor modulator” intends and encompasses a compound that binds to or inhibits binding of a ligand to a dopamine receptor or reduces or eliminates or increases or enhances or mimics an activity of a dopamine receptor. As such, a “dopamine receptor modulator” encompasses both a dopamine receptor antagonist and a dopamine receptor agonist. In some aspects, the dopamine receptor modulator binds to or inhibits binding of a ligand to a dopamine-1 (D1) and/or a dopamine-2 (D2) receptor or reduces or eliminates or increases or enhances or mimics an activity of a dopamine-1 (D1) and/or a dopamine-2 (D2) receptor in a reversible or irreversible manner. Dopamine D2 receptors are divided into two categories, D2L and D2S, which are formed from a single gene by differential splicing. D2L receptors have a longer intracellular domain than D2S. In some embodiments, the dopamine receptor modulator inhibits binding of a ligand by at least about or about any one of 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 100% as determined in the assays described herein. In some embodiments, the dopamine receptor modulator reduces an activity of a dopamine receptor by at least about or about any of 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 100% as compared to the corresponding activity in the same subject prior to treatment with the dopamine receptor modulator or compared to the corresponding activity in other subjects not receiving the dopamine receptor modulator. In some embodiments, the dopamine receptor modulator enhances an activity of a dopamine receptor by at least about or about any of 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 100 or 200% or 300% or 400% or 500% or more as compared to the corresponding activity in the same subject prior to treatment with the dopamine receptor modulator or compared to the corresponding activity in other subjects not receiving the dopamine receptor modulator. In some embodiments, the dopamine receptor modulator is capable of binding to the active site of a dopamine receptor (e.g., a binding site for a ligand). In some embodiments, the dopamine receptor modulator is capable of binding to an allosteric site of a dopamine receptor.

As used herein, the term “serotonin receptor modulator” intends and encompasses a compound that binds to or inhibits binding of a ligand to a serotonin receptor or reduces or eliminates or increases or enhances or mimics an activity of a serotonin receptor. As such, a “serotonin receptor modulator” encompasses both a serotonin receptor antagonist and a serotonin receptor agonist. In some embodiments, the serotonin receptor modulator binds to or inhibits binding of a ligand to a 5-HT1A and/or a 5-HT1B and/or a 5-HT2A and/or a 5-HT2B and/or a 5-HT2C and/or a 5-HT3 and/or a 5-HT4 and/or a 5-HT6 and/or a 5-HT7 receptor or reduces or eliminates or increases or enhances or mimics an activity of a 5-HT1A and/or a 5-HT1B and/or a 5-HT2A and/or a 5-HT2B and/or a 5-HT2C and/or a 5-HT3 and/or a 5-HT4 and/or a 5-HT6 and/or a 5-HT7 receptor in a reversible or irreversible manner. In some embodiments, the serotonin receptor modulator inhibits binding of a ligand by at least about or about any one of 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 100% as determined in the assays described herein. In some embodiments, the serotonin receptor modulator reduces an activity of a serotonin receptor by at least about or about any of 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 100% as compared to the corresponding activity in the same subject prior to treatment with the serotonin receptor modulator or compared to the corresponding activity in other subjects not receiving the serotonin receptor modulator. In some embodiments, the serotonin receptor modulator enhances an activity of a serotonin receptor by at least about or about any of 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 100 or 200% or 300% or 400% or 500% or more as compared to the corresponding activity in the same subject prior to treatment with the serotonin receptor modulator or compared to the corresponding activity in other subjects not receiving the serotonin receptor modulator. In some embodiments, the serotonin receptor modulator is capable of binding to the active site of a serotonin receptor (e.g., a binding site for a ligand). In some embodiments, the serotonin receptor modulator is capable of binding to an allosteric site of a serotonin receptor.

As used herein, the term “histamine receptor modulator” intends and encompasses a compound that binds to or inhibits binding of a ligand to a histamine receptor or reduces or eliminates or increases or enhances or mimics an activity of a histamine receptor. As such, a “histamine receptor modulator” encompasses both a histamine receptor antagonist and a histamine receptor agonist. In some embodiments, the histamine receptor modulator binds to or inhibits binding of a ligand to a histamine H1 and/or H2 and/or H3 receptor or reduces or eliminates or increases or enhances or mimics an activity of a histamine H1 and/or H2 and/or H3 receptor in a reversible or irreversible manner. In some embodiments, the histamine receptor modulator inhibits binding of a ligand by at least about or about any one of 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 100% as determined in the assays described herein. In some embodiments, the histamine receptor modulator reduces an activity of a histamine receptor by at least about or about any of 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 100% as compared to the corresponding activity in the same subject prior to treatment with the histamine receptor modulator or compared to the corresponding activity in other subjects not receiving the histamine receptor modulator. In some embodiments, the histamine receptor modulator enhances an activity of a histamine receptor by at least about or about any of 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 100 or 200% or 300% or 400% or 500% or more as compared to the corresponding activity in the same subject prior to treatment with the histamine receptor modulator or compared to the corresponding activity in other subjects not receiving the histamine receptor modulator. In some embodiments, the histamine receptor modulator is capable of binding to the active site of a histamine receptor (e.g., a binding site for a ligand). In some embodiments, the histamine receptor modulator is capable of binding to an allosteric site of a histamine receptor.

Unless clearly indicated otherwise, “an individual” as used herein intends a mammal, including but not limited to human, bovine, primate, equine, canine, feline, porcine, and ovine animals. Thus, the invention finds use in both human medicine and in the veterinary context, including use in agricultural animals and domestic pets. The individual may be a human who has been diagnosed with or is suspected of having a cognitive disorder, a psychotic disorder, a neurotransmitter-mediated disorder and/or a neuronal disorder. The individual may be a human who exhibits one or more symptoms associated with a cognitive disorder, a psychotic disorder, a neurotransmitter-mediated disorder and/or a neuronal disorder. The individual may be a human who has a mutated or abnormal gene associated with a cognitive disorder, a psychotic disorder, a neurotransmitter-mediated disorder and/or a neuronal disorder. The individual may be a human who is genetically or otherwise predisposed to developing a cognitive disorder, a psychotic disorder, a neurotransmitter-mediated disorder and/or a neuronal disorder.

As used herein, “treatment” or “treating” is an approach for obtaining beneficial or desired results, including clinical results. For purposes of this invention, beneficial or desired clinical results include, but are not limited to, alleviation of a symptom and/or diminishment of the extent of a symptom and/or preventing a worsening of a symptom associated with a disease or condition. In one variation, beneficial or desired clinical results include, but are not limited to, alleviation of a symptom and/or diminishment of the extent of a symptom and/or preventing a worsening of a symptom associated with a cognitive disorder, a psychotic disorder, a neurotransmitter-mediated disorder and/or a neuronal disorder. Preferably, treatment of a disease or condition with a compound of the invention or a pharmaceutically acceptable salt thereof is accompanied by no or fewer side effects than are associated with currently available therapies for the disease or condition and/or improves the quality of life of the individual.

As used herein, “delaying” development of a disease or condition means to defer, hinder, slow, retard, stabilize and/or postpone development of the disease or condition. This delay can be of varying lengths of time, depending on the history of the disease and/or individual being treated. As is evident to one skilled in the art, a sufficient or significant delay can, in effect, encompass prevention, in that the individual does not develop the disease or condition. For example, a method that “delays” development of Alzheimer's disease is a method that reduces probability of disease development in a given time frame and/or reduces extent of the disease in a given time frame, when compared to not using the method. Such comparisons are typically based on clinical studies, using a statistically significant number of subjects. For example, Alzheimer's disease development can be detected using standard clinical techniques, such as routine neurological examination, patient interview, neuroimaging, detecting alterations of levels of specific proteins in the serum or cerebrospinal fluid (e.g., amyloid peptides and Tau), computerized tomography (CT) or magnetic resonance imaging (MRI). Similar techniques are known in the art for other diseases and conditions. Development may also refer to disease progression that may be initially undetectable and includes occurrence, recurrence and onset.

As used herein, an “at risk” individual is an individual who is at risk of developing a cognitive disorder, a psychotic disorder, a neurotransmitter-mediated disorder and/or a neuronal disorder that can be treated with a compound of the invention. An individual “at risk” may or may not have a detectable disease or condition, and may or may not have displayed detectable disease prior to the treatment methods described herein. “At risk” denotes that an individual has one or more so-called risk factors, which are measurable parameters that correlate with development of a disease or condition and are known in the art. An individual having one or more of these risk factors has a higher probability of developing the disease or condition than an individual without these risk factor(s). These risk factors include, but are not limited to, age, sex, race, diet, history of previous disease, presence of precursor disease, genetic (i.e., hereditary) considerations, and environmental exposure. For example, individuals at risk for Alzheimer's disease include, e.g., those having relatives who have experienced this disease and those whose risk is determined by analysis of genetic or biochemical markers. Genetic markers of risk for Alzheimer's disease include mutations in the APP gene, particularly mutations at position 717 and positions 670 and 671 referred to as the Hardy and Swedish mutations, respectively (Hardy, Trends Neurosci., 20:154-9, 1997). Other markers of risk are mutations in the presenilin genes (e.g., PS1 or PS2), ApoE4 alleles, family history of Alzheimer's disease, hypercholesterolemia and/or atherosclerosis. Other such factors are known in the art for other diseases and conditions.

As used herein, the term “pro-cognitive” includes but is not limited to an improvement of one or more mental processes such as memory, attention, perception and/or thinking, which may be assessed by methods known in the art.

As used herein, the term “neurotrophic” effects includes but is not limited to effects that enhance neuron function such as growth, survival and/or neurotransmitter synthesis.

As used herein, the term “cognitive disorders” refers to and intends diseases and conditions that are believed to involve or be associated with or do involve or are associated with progressive loss of structure and/or function of neurons, including death of neurons, and where a central feature of the disorder may be the impairment of cognition (e.g., memory, attention, perception and/or thinking). These disorders include pathogen-induced cognitive dysfunction, e.g. HIV associated cognitive dysfunction and Lyme disease associated cognitive dysfunction. Examples of cognitive disorders include Alzheimer's Disease, Huntington's Disease, Parkinson's Disease, amyotrophic lateral sclerosis (ALS), autism, mild cognitive impairment (MCI), stroke, traumatic brain injury (TBI) and age-associated memory impairment (AAMI).

As used herein, the term “psychotic disorders” refers to and intends mental diseases or conditions that are believed to cause or do cause abnormal thinking and perceptions. Psychotic disorders are characterized by a loss of reality which may be accompanied by delusions, hallucinations (perceptions in a conscious and awake state in the absence of external stimuli which have qualities of real perception, in that they are vivid, substantial, and located in external objective space), personality changes and/or disorganized thinking. Other common symptoms include unusual or bizarre behavior, as well as difficulty with social interaction and impairment in carrying out the activities of daily living. Exemplary psychotic disorders are schizophrenia, bipolar disorders, psychosis, anxiety and depression.

As used herein, the term “neurotransmitter-mediated disorders” refers to and intends diseases or conditions that are believed to involve or be associated with or do involve or are associated with abnormal levels of neurotransmitters such as histamine, serotonin, dopamine, norepinephrine or impaired function of aminergic G protein-coupled receptors. Exemplary neurotransmitter-mediated disorders include spinal cord injury, diabetic neuropathy, allergic diseases and diseases involving geroprotective activity such as age-associated hair loss (alopecia), age-associated weight loss and age-associated vision disturbances (cataracts). Abnormal neurotransmitter levels are associated with a wide variety of diseases and conditions including, but not limited, to Alzheimer's disease, Parkinson's Disease, autism, Guillain-Barré syndrome, mild cognitive impairment, schizophrenia, anxiety, multiple sclerosis, stroke, traumatic brain injury, spinal cord injury, diabetic neuropathy, fibromyalgia, bipolar disorders, psychosis, depression and a variety of allergic diseases.

As used herein, the term “neuronal disorders” refers to and intends diseases or conditions that are believed to involve, or be associated with, or do involve or are associated with neuronal cell death and/or impaired neuronal function or decreased neuronal function. Exemplary neuronal indications include neurodegenerative diseases and disorders such as Alzheimer's disease, Huntington's disease, amyotrophic lateral sclerosis (ALS), Parkinson's disease, canine cognitive dysfunction syndrome (CCDS), Lewy body disease, Menkes disease, Wilson disease, Creutzfeldt-Jakob disease, Fahr disease, an acute or chronic disorder involving cerebral circulation, such as ischemic or hemorrhagic stroke or other cerebral hemorrhagic insult, age-associated memory impairment (AAMI), mild cognitive impairment (MCI), injury-related mild cognitive impairment (MCI), post-concussion syndrome, post-traumatic stress disorder, adjuvant chemotherapy, traumatic brain injury (TBI), neuronal death mediated ocular disorder, macular degeneration, age-related macular degeneration, autism, including autism spectrum disorder, Asperger syndrome, and Rett syndrome, an avulsion injury, a spinal cord injury, myasthenia gravis, Guillain-Barré syndrome, multiple sclerosis, diabetic neuropathy, fibromyalgia, neuropathy associated with spinal cord injury, schizophrenia, bipolar disorder, psychosis, anxiety or depression.

As used herein, the term “neuron” represents a cell of ectodermal embryonic origin derived from any part of the nervous system of an animal. Neurons express well-characterized neuron-specific markers, including neurofilament proteins, NeuN (Neuronal Nuclei marker), MAP2, and class III tubulin. Included as neurons are, for example, hippocampal, cortical, midbrain dopaminergic, spinal motor, sensory, sympathetic, septal cholinergic, and cerebellar neurons.

As used herein, the term “neurite outgrowth” or “neurite activation” refers to the extension of existing neuronal processes (e.g., axons and dendrites) and the growth or sprouting of new neuronal processes (e.g., axons and dendrites). Neurite outgrowth or neurite activation may alter neural connectivity, resulting in the establishment of new synapses or the remodeling of existing synapses.

As used herein, the term “neurogenesis” refers to the generation of new nerve cells from undifferentiated neuronal progenitor cells, also known as multipotential neuronal stem cells. Neurogenesis actively produces new neurons, astrocytes, glia, Schwann cells, oligodendrocytes and/or other neural lineages. Much neurogenesis occurs early in human development, though it continues later in life, particularly in certain localized regions of the adult brain.

As used herein, the term “neural connectivity” refers to the number, type, and quality of connections (“synapses”) between neurons in an organism. Synapses form between neurons, between neurons and muscles (a “neuromuscular junction”), and between neurons and other biological structures, including internal organs, endocrine glands, and the like. Synapses are specialized structures by which neurons transmit chemical or electrical signals to each other and to non-neuronal cells, muscles, tissues, and organs. Compounds that affect neural connectivity may do so by establishing new synapses (e.g., by neurite outgrowth or neurite activation) or by altering or remodeling existing synapses. Synaptic remodeling refers to changes in the quality, intensity or type of signal transmitted at particular synapses.

As used herein, the term “neuropathy” refers to a disorder characterized by altered function and/or structure of motor, sensory, and autonomic neurons of the nervous system, initiated or caused by a primary lesion or other dysfunction of the nervous system. Patterns of peripheral neuropathy include polyneuropathy, mononeuropathy, mononeuritis multiplex and autonomic neuropathy. The most common form is (symmetrical) peripheral polyneuropathy, which mainly affects the feet and legs. A radiculopathy involves spinal nerve roots, but if peripheral nerves are also involved the term radiculoneuropathy is used. The form of neuropathy may be further broken down by cause, or the size of predominant fiber involvement, e.g. large fiber or small fiber peripheral neuropathy. Central neuropathic pain can occur in spinal cord injury, multiple sclerosis, and some strokes, as well as fibromyalgia. Neuropathy may be associated with varying combinations of weakness, autonomic changes and sensory changes. Loss of muscle bulk or fasciculations, a particular fine twitching of muscle may also be seen. Sensory symptoms encompass loss of sensation and “positive” phenomena including pain. Neuropathies are associated with a variety of disorders, including diabetes (e.g., diabetic neuropathy), fibromyalgia, multiple sclerosis, and herpes zoster infection, as well as with spinal cord injury and other types of nerve damage.

As used herein, the term “Alzheimer's disease” refers to a degenerative brain disorder characterized clinically by progressive memory deficits, confusion, behavioral problems, inability to care for oneself, gradual physical deterioration and, ultimately, death. Histologically, the disease is characterized by neuritic plaques, found primarily in the association cortex, limbic system and basal ganglia. The major constituent of these plaques is amyloid beta peptide (Aβ), which is the cleavage product of beta amyloid precursor protein (βAPP or APP). APP is a type I transmembrane glycoprotein that contains a large ectopic N-terminal domain, a transmembrane domain and a small cytoplasmic C-terminal tail. Alternative splicing of the transcript of the single APP gene on chromosome 21 results in several isoforms that differ in the number of amino acids. Aβ appears to have a central role in the neuropathology of Alzheimer's disease. Familial forms of the disease have been linked to mutations in APP and the presenilin genes (Tanzi et al., 1996, Neurobiol. Dis., 3:159-168; Hardy, 1996, Ann. Med., 28:255-258). Diseased-linked mutations in these genes result in increased production of the 42-amino acid form of Aβ, the predominant form found in amyloid plaques. Mitochondrial dysfunction has also been reported to be an important component of Alzheimer's disease (Bubber et al., Mitochondrial abnormalities in Alzheimer brain: Mechanistic Implications, Ann Neurol., 2005, 57(5), 695-703; Wang et al., Insights into amyloid-β-induced mitochondrial dysfunction in Alzheimer disease, Free Radical Biology & Medicine, 2007, 43, 1569-1573; Swerdlow et al., Mitochondria in Alzheimer's disease, Int. Rev. Neurobiol., 2002, 53, 341-385; and Reddy et al., Are mitochondria critical in the pathogenesis of Alzheimer's disease?, Brain Res Rev. 2005, 49(3), 618-32). It has been proposed that mitochondrial dysfunction has a causal relationship with neuronal function (including neurotransmitter synthesis and secretion) and viability. Compounds which stabilize mitochondria may therefore have a beneficial impact on Alzheimer's patients.

As used herein, the term “Huntington's disease” refers to a fatal neurological disorder characterized clinically by symptoms such as involuntary movements, cognition impairment or loss of cognitive function and a wide spectrum of behavioral disorders. Common motor symptoms associated with Huntington's disease include chorea (involuntary writhing and spasming), clumsiness, and progressive loss of the abilities to walk, speak (e.g., exhibiting slurred speech) and swallow. Other symptoms of Huntington's disease can include cognitive symptoms such as loss of intellectual speed, attention and short-term memory and/or behavioral symptoms that can span the range of changes in personality, depression, irritability, emotional outbursts and apathy. Clinical symptoms typically appear in the fourth or fifth decade of life. Huntington's disease is a devastating and often protracted illness, with death usually occurring approximately 10-20 years after the onset of symptoms. Huntington's disease is inherited through a mutated or abnormal gene encoding an abnormal protein called the mutant huntingtin protein; the mutated huntingtin protein produces neuronal degeneration in many different regions of the brain. The degeneration focuses on neurons located in the basal ganglia, structures deep within the brain that control many important functions including coordinating movement, and on neurons on the outer surface of the brain or cortex, which controls thought, perception and memory.

“Amyotrophic lateral sclerosis” or “ALS” are used herein to denote a progressive neurodegenerative disease that affects upper motor neurons (motor neurons in the brain) and/or lower motor neurons (motor neurons in the spinal cord) and results in motor neuron death. As used herein, the term “ALS” includes all of the classifications of ALS known in the art, including, but not limited to classical ALS (typically affecting both lower and upper motor neurons), Primary Lateral Sclerosis (PLS, typically affecting only the upper motor neurons), Progressive Bulbar Palsy (PBP or Bulbar Onset, a version of ALS that typically begins with difficulties swallowing, chewing and speaking), Progressive Muscular Atrophy (PMA, typically affecting only the lower motor neurons) and familial ALS (a genetic version of ALS).

The term “Parkinson's disease” as used herein refers to any medical condition wherein an individual experiences one or more symptoms associated with Parkinson's disease, such as without limitation one or more of the following symptoms: rest tremor, cogwheel rigidity, bradykinesia, postural reflex impairment, symptoms having good response to 1-dopa treatment, the absence of prominent oculomotor palsy, cerebellar or pyramidal signs, amyotrophy, dyspraxia and/or dysphasia. In a specific embodiment, the present invention is utilized for the treatment of a dopaminergic dysfunction-related disorder. In a specific embodiment, the individual with Parkinson's disease has a mutation or polymorphism in a synuclein, parkin or NURR1 nucleic acid that is associated with Parkinson's disease. In one embodiment, the individual with Parkinson's disease has defective or decreased expression of a nucleic acid or a mutation in a nucleic acid that regulates the development and/or survival of dopaminergic neurons.

As used herein, the term “canine cognitive dysfunction syndrome,” or “CCDS” refers to an age-related deterioration of mental function typified by multiple cognitive impairments that affect an afflicted canine's ability to function normally. The decline in cognitive ability that is associated with CCDS cannot be completely attributed to a general medical condition such as neoplasia, infection, sensory impairment, or organ failure. Diagnosis of CCDS in canines, such as dogs, is generally a diagnosis of exclusion, based on thorough behavior and medical histories and the presence of clinical symptoms of CCDS that are unrelated to other disease processes. Owner observation of age-related changes in behavior is a practical means used to detect the possible onset of CCDS in aging domestic dogs. A number of laboratory cognitive tasks may be used to help diagnose CCDS, while blood counts, chemistry panels and urinalysis can be used to rule out other underlying diseases that could mimic the clinical symptoms of CCDS. Symptoms of CCDS include memory loss, which in domestic dogs may be manifested by disorientation and/or confusion, decreased or altered interaction with family members and/or greeting behavior, changes in sleep-wake cycle, decreased activity level, and loss of house training or frequent, inappropriate elimination. A canine suffering from CCDS may exhibit one or more of the following clinical or behavioral symptoms: decreased appetite, decreased awareness of surroundings, decreased ability to recognize familiar places, people or other animals, decreased hearing, decreased ability to climb up and down stairs, decreased tolerance to being alone, development of compulsive behavior or repetitive behaviors or habits, circling, tremors or shaking, disorientation, decreased activity level, abnormal sleep wake cycles, loss of house training, decreased or altered responsiveness to family members, and decreased or altered greeting behavior. CCDS can dramatically affect the health and well-being of an afflicted canine. Moreover, the companionship offered by a pet with CCDS can become less rewarding as the severity of the disease increases and its symptoms become more severe.

As used herein, the term “age-associated memory impairment” or “AAMI” refers to a condition that may be identified as GDS stage 2 on the global deterioration scale (GDS) (Reisberg, et al. (1982) Am. J. Psychiatry 139: 1136-1139) which differentiates the aging process and progressive degenerative dementia in seven major stages. The first stage of the GDS is one in which individuals at any age have neither subjective complaints of cognitive impairment nor objective evidence of impairment. These GDS stage 1 individuals are considered normal. The second stage of the GDS applies to those generally elderly persons who complain of memory and cognitive functioning difficulties such as not recalling names as well as they could five or ten years previously or not recalling where they have placed things as well as they could five or ten years previously. These subjective complaints appear to be very common in otherwise normal elderly individuals. AAMI refers to persons in GDS stage 2, who may differ neurophysiologically from elderly persons who are normal and free of subjective complaints, i.e., GDS stage 1. For example, AAMI subjects have been found to have more electrophysiologic slowing on a computer analyzed EEG than GDS stage 1 elderly persons (Prichep, John, Ferris, Reisberg, et al., (1994) Neurobiol. Aging 15: 85-90).

As used herein, the term “mild cognitive impairment” or “MCI” refers to a type of cognitive disorder characterized by a more pronounced deterioration in cognitive functions than is typical for normal age-related decline. As a result, elderly or aged patients with MCI have greater than normal difficulty performing complex daily tasks and learning, but without the inability to perform normal social, everyday, and/or professional functions typical of patients with Alzheimer's disease, or other similar neurodegenerative disorders eventually resulting in dementia. MCI is characterized by subtle, clinically manifest deficits in cognition, memory, and functioning, amongst other impairments, which are not of sufficient magnitude to fulfill criteria for diagnosis of Alzheimer's disease or other dementia. MCI also encompasses injury-related MCI, defined herein as cognitive impairment resulting from certain types of injury, such as nerve injury (i.e., battlefield injuries, including post-concussion syndrome, and the like), neurotoxic treatment (i.e., adjuvant chemotherapy resulting in “chemo brain” and the like), and tissue damage resulting from physical injury or other neurodegeneration, which is separate and distinct from mild cognitive impairment resulting from stroke, ischemia, hemorrhagic insult, blunt force trauma, and the like.

As used herein, the term “traumatic brain injury” or “TBI” refers to a brain injury caused by a sudden trauma, such as a blow or jolt or a penetrating head injury, which disrupts the function or damages the brain. Symptoms of TBI can range from mild, moderate to severe and can significantly affect many cognitive (deficits of language and communication, information processing, memory, and perceptual skills), physical (ambulation, balance, coordination, fine motor skills, strength, and endurance), and psychological skills.

“Neuronal death mediated ocular disease” intends an ocular disease in which death of the neuron is implicated in whole or in part. The disease may involve death of photoreceptors. The disease may involve retinal cell death. The disease may involve ocular nerve death by apoptosis. Particular neuronal death mediated ocular diseases include but are not limited to macular degeneration, glaucoma, retinitis pigmentosa, congenital stationary night blindness (Oguchi disease), childhood onset severe retinal dystrophy, Leber congenital amaurosis, Bardet-Biedle syndrome, Usher syndrome, blindness from an optic neuropathy, Leber's hereditary optic neuropathy, color blindness and Hansen-Larson-Berg syndrome.

As used herein, the term “macular degeneration” includes all forms and classifications of macular degeneration known in the art, including, but not limited to diseases that are characterized by a progressive loss of central vision associated with abnormalities of Bruch's membrane, the choroid, the neural retina and/or the retinal pigment epithelium. The term thus encompasses disorders such as age-related macular degeneration (ARMD) as well as rarer, earlier-onset dystrophies that in some cases can be detected in the first decade of life. Other maculopathies include North Carolina macular dystrophy, Sorsby's fundus dystrophy, Stargardt's disease, pattern dystrophy, Best disease, and Malattia Leventinese.

As used herein, the term “autism” refers to a brain development disorder that impairs social interaction and communication and causes restricted and repetitive behavior, typically appearing during infancy or early childhood. The cognitive and behavioral defects are thought to result in part from altered neural connectivity. Autism encompasses related disorders sometimes referred to as “autism spectrum disorder,” as well as Asperger syndrome and Rett syndrome.

As used herein, the term “nerve injury” or “nerve damage” refers to physical damage to nerves, such as avulsion injury (i.e., where a nerve or nerves have been torn or ripped) or spinal cord injury (i.e., damage to white matter or myelinated fiber tracts that carry sensation and motor signals to and from the brain). Spinal cord injury can occur from many causes, including physical trauma (i.e., car accidents, sports injuries, and the like), tumors impinging on the spinal column, developmental disorders, such as spina bifida, and the like.

As used herein, the term “myasthenia gravis” or “MG” refers to a non-cognitive neuromuscular disorder caused by immune-mediated loss of acetylcholine receptors at neuromuscular junctions of skeletal muscle. Clinically, MG typically appears first as occasional muscle weakness in approximately two-thirds of patients, most commonly in the extraocular muscles. These initial symptoms eventually worsen, producing drooping eyelids (ptosis) and/or double vision (diplopia), often causing the patient to seek medical attention. Eventually, many patients develop general muscular weakness that may fluctuate weekly, daily, or even more frequently. Generalized MG often affects muscles that control facial expression, chewing, talking, swallowing, and breathing; before recent advances in treatment, respiratory failure was the most common cause of death.

As used herein, the term “Guillain-Barré syndrome” refers to a non-cognitive disorder in which the body's immune system attacks part of the peripheral nervous system. The first symptoms of this disorder include varying degrees of weakness or tingling sensations in the legs. In many instances the weakness and abnormal sensations spread to the arms and upper body. These symptoms can increase in intensity until certain muscles cannot be used at all and, when severe, the patient is almost totally paralyzed. In these cases the disorder is life threatening—potentially interfering with breathing and, at times, with blood pressure or heart rate—and is considered a medical emergency. Most patients, however, recover from even the most severe cases of Guillain-Barré syndrome, although some continue to have a certain degree of weakness.

As used herein, the term “multiple sclerosis” or “MS” refers to an autoimmune condition in which the immune system attacks the central nervous system (CNS), leading to demyelination of neurons. It may cause numerous symptoms, many of which are non-cognitive, and often progresses to physical disability. MS affects the areas of the brain and spinal cord known as the white matter. White matter cells carry signals between the grey matter areas, where the processing is done, and the rest of the body. More specifically, MS destroys oligodendrocytes which are the cells responsible for creating and maintaining a fatty layer, known as the myelin sheath, which helps the neurons carry electrical signals. MS results in a thinning or complete loss of myelin and, less frequently, the cutting (transection) of the neuron's extensions or axons. When the myelin is lost, the neurons can no longer effectively conduct their electrical signals. Almost any neurological symptom can accompany the disease. MS takes several forms, with new symptoms occurring either in discrete attacks (relapsing forms) or slowly accumulating over time (progressive forms). Most people are first diagnosed with relapsing-remitting MS but develop secondary-progressive MS (SPMS) after a number of years. Between attacks, symptoms may go away completely, but permanent neurological problems often persist, especially as the disease advances.

As used herein, the term “schizophrenia” refers to a chronic, mental disorder characterized by one or more positive symptoms (e.g., delusions and hallucinations) and/or negative symptoms (e.g., blunted emotions and lack of interest) and/or disorganized symptoms (e.g., disorganized thinking and speech or disorganized perception and behavior). Schizophrenia as used herein includes all forms and classifications of schizophrenia known in the art, including, but not limited to catatonic type, hebephrenic type, disorganized type, paranoid type, residual type or undifferentiated type schizophrenia and deficit syndrome and/or those described in American Psychiatric Association: Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Washington D.C., 2000 or in International Statistical Classification of Diseases and Related Health Problems, or otherwise known to those of skill in the art.

As used herein “geroprotective activity” or “geroprotector” means a biological activity that slows down ageing and/or prolongs life and/or increases or improves the quality of life via a decrease in the amount and/or the level of intensity of pathologies or conditions that are not life-threatening but are associated with the aging process and which are typical for elderly people. Pathologies or conditions that are not life-threatening but are associated with the aging process include such pathologies or conditions as loss of sight (cataract), deterioration of the dermatohairy integument (alopecia), and an age-associated decrease in weight due to the death of muscular and/or fatty cells.

As used herein “allergic disease” refers to a disorder of the immune system which is characterized by excessive activation of mast cells and basophils and production of IgE immunoglobulins, resulting in an extreme inflammatory response. It represents a form of hypersensitivity to an environmental substance known as allergen and is an acquired disease. Common allergic reactions include eczema, hives, hay fever, asthma, food allergies, and reactions to the venom of stinging insects such as wasps and bees. Allergic reactions are accompanied by an excessive release of histamines, and can thus be treated with antihistaminic agents.

As used herein, by “combination therapy” is meant a therapy that includes two or more different compounds. Thus, in one aspect, a combination therapy comprising a compound detailed herein and anther compound is provided. In some variations, the combination therapy optionally includes one or more pharmaceutically acceptable carriers or excipients, non-pharmaceutically active compounds, and/or inert substances. In various embodiments, treatment with a combination therapy may result in an additive or even synergistic (e.g., greater than additive) result compared to administration of a single compound of the invention alone. In some embodiments, a lower amount of each compound is used as part of a combination therapy compared to the amount generally used for individual therapy. Preferably, the same or greater therapeutic benefit is achieved using a combination therapy than by using any of the individual compounds alone. In some embodiments, the same or greater therapeutic benefit is achieved using a smaller amount (e.g., a lower dose or a less frequent dosing schedule) of a compound in a combination therapy than the amount generally used for individual compound or therapy. Preferably, the use of a small amount of compound results in a reduction in the number, severity, frequency, and/or duration of one or more side-effects associated with the compound.

As used herein, the term “effective amount” intends such amount of a compound of the invention which in combination with its parameters of efficacy and toxicity, as well as based on the knowledge of the practicing specialist should be effective in a given therapeutic form. As is understood in the art, an effective amount may be in one or more doses, i.e., a single dose or multiple doses may be required to achieve the desired treatment endpoint. An effective amount may be considered in the context of administering one or more therapeutic agents, and a single agent may be considered to be given in an effective amount if, in conjunction with one or more other agents, a desirable or beneficial result may be or is achieved. Suitable doses of any of the co-administered compounds may optionally be lowered due to the combined action (e.g., additive or synergistic effects) of the compounds.

As used herein, “unit dosage form” refers to physically discrete units, suitable as unit dosages, each unit containing a predetermined quantity of active ingredient calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. Unit dosage forms may contain a single or a combination therapy.

As used herein, the term “controlled release” refers to a drug-containing formulation or fraction thereof in which release of the drug is not immediate, i.e., with a “controlled release” formulation, administration does not result in immediate release of the drug into an absorption pool. The term encompasses depot formulations designed to gradually release the drug compound over an extended period of time. Controlled release formulations can include a wide variety of drug delivery systems, generally involving mixing the drug compound with carriers, polymers or other compounds having the desired release characteristics (e.g., pH-dependent or non-pH-dependent solubility, different degrees of water solubility, and the like) and formulating the mixture according to the desired route of delivery (e.g., coated capsules, implantable reservoirs, injectable solutions containing biodegradable capsules, and the like).

As used herein, by “pharmaceutically acceptable” or “pharmacologically acceptable” is meant a material that is not biologically or otherwise undesirable, e.g., the material may be incorporated into a pharmaceutical composition administered to a patient without causing any significant undesirable biological effects or interacting in a deleterious manner with any of the other components of the composition in which it is contained. Pharmaceutically acceptable carriers or excipients have preferably met the required standards of toxicological and manufacturing testing and/or are included on the Inactive Ingredient Guide prepared by the U.S. Food and Drug administration.

“Pharmaceutically acceptable salts” are those salts which retain at least some of the biological activity of the free (non-salt) compound and which can be administered as drugs or pharmaceuticals to an individual. A pharmaceutically acceptable salt intends ionic interactions and not a covalent bond. As such, an N-oxide is not considered a salt. Such salts, for example, include: (1) acid addition salts, formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like; or formed with organic acids such as acetic acid, oxalic acid, propionic acid, succinic acid, maleic acid, tartaric acid and the like; (2) salts formed when an acidic proton present in the parent compound either is replaced by a metal ion, e.g., an alkali metal ion, an alkaline earth ion, or an aluminum ion; or coordinates with an organic base. Acceptable organic bases include ethanolamine, diethanolamine, triethanolamine and the like. Acceptable inorganic bases include aluminum hydroxide, calcium hydroxide, potassium hydroxide, sodium carbonate, sodium hydroxide, and the like. Further examples of pharmaceutically acceptable salts include those listed in Berge et al., Pharmaceutical Salts, J. Pharm. Sci. 1977 January; 66(1):1-19. Pharmaceutically acceptable salts can be prepared in situ in the manufacturing process, or by separately reacting a purified compound of the invention in its free acid or base form with a suitable organic or inorganic base or acid, respectively, and isolating the salt thus formed during subsequent purification. It should be understood that a reference to a pharmaceutically acceptable salt includes the solvent addition forms or crystal forms thereof, particularly solvates or polymorphs. Solvates contain either stoichiometric or non-stoichiometric amounts of a solvent, and are often formed during the process of crystallization. Hydrates are formed when the solvent is water, or alcoholates are formed when the solvent is alcohol. Polymorphs include the different crystal packing arrangements of the same elemental composition of a compound. Polymorphs usually have different X-ray diffraction patterns, infrared spectra, melting points, density, hardness, crystal shape, optical and electrical properties, stability, and solubility. Various factors such as the recrystallization solvent, rate of crystallization, and storage temperature may cause a single crystal form to dominate.

The term “excipient” as used herein means an inert or inactive substance that may be used in the production of a drug or pharmaceutical, such as a tablet containing a compound of the invention as an active ingredient. Various substances may be embraced by the term excipient, including without limitation any substance used as a binder, disintegrant, coating, compression/encapsulation aid, cream or lotion, lubricant, solutions for parenteral administration, materials for chewable tablets, sweetener or flavoring, suspending/gelling agent, or wet granulation agent. Binders include, e.g., carbomers, povidone, xanthan gum, etc.; coatings include, e.g., cellulose acetate phthalate, ethylcellulose, gellan gum, maltodextrin, enteric coatings, etc.; compression/encapsulation aids include, e.g., calcium carbonate, dextrose, fructose dc (dc=“directly compressible”), honey dc, lactose (anhydrate or monohydrate; optionally in combination with aspartame, cellulose, or microcrystalline cellulose), starch dc, sucrose, etc.; disintegrants include, e.g., croscarmellose sodium, gellan gum, sodium starch glycolate, etc.; creams or lotions include, e.g., maltodextrin, carrageenans, etc.; lubricants include, e.g., magnesium stearate, stearic acid, sodium stearyl fumarate, etc.; materials for chewable tablets include, e.g., dextrose, fructose dc, lactose (monohydrate, optionally in combination with aspartame or cellulose), etc.; suspending/gelling agents include, e.g., carrageenan, sodium starch glycolate, xanthan gum, etc.; sweeteners include, e.g., aspartame, dextrose, fructose dc, sorbitol, sucrose dc, etc.; and wet granulation agents include, e.g., calcium carbonate, maltodextrin, microcrystalline cellulose, etc.

“Alkyl” refers to and includes saturated linear, branched, or cyclic univalent hydrocarbon structures and combinations thereof. Particular alkyl groups are those having 1 to 20 carbon atoms (a “C₁-C₂₀ alkyl”). More particular alkyl groups are those having 1 to 8 carbon atoms (a “C₁-C₈ alkyl”). When an alkyl residue having a specific number of carbons is named, all geometric isomers having that number of carbons are intended to be encompassed and described; thus, for example, “butyl” is meant to include n-butyl, sec-butyl, iso-butyl, tert-butyl and cyclobutyl; “propyl” includes n-propyl, iso-propyl and cyclopropyl. This term is exemplified by groups such as methyl, t-butyl, n-heptyl, octyl, cyclohexylmethyl, cyclopropyl and the like. Cycloalkyl is a subset of alkyl and can consist of one ring, such as cyclohexyl, or multiple rings, such as adamantyl. A cycloalkyl comprising more than one ring may be fused, spiro or bridged, or combinations thereof. In fused ring systems, one or more of the rings can be aryl or heteroaryl. A cycloalkyl having more than one ring where at least one ring is aromatic may be connected to the parent structure at either a non-aromatic ring position or at an aromatic ring position. In one variation, a cycloalkyl having more than one ring where at least one ring is aromatic is connected to the parent structure at a non-aromatic ring position. A preferred cycloalkyl is a saturated cyclic hydrocarbon having from 3 to 13 annular carbon atoms. A more preferred cycloalkyl is a saturated cyclic hydrocarbon having from 3 to 7 annular carbon atoms (a “C₃-C₇ cycloalkyl”). Examples of cycloalkyl groups include adamantyl, decahydronaphthalenyl, cyclopropyl, cyclobutyl, cyclopentyl and the like.

“Alkylene” refers to the same residues as alkyl, but having bivalency. Examples of alkylene include ethylene (—CH₂CH₂—) and propylene (—CH₂CH₂CH₂—).

“Alkenyl” refers to an unsaturated hydrocarbon group having at least one site of olefinic unsaturation (i.e., having at least one moiety of the formula C═C) and preferably having from 2 to 10 carbon atoms and more preferably 2 to 8 carbon atoms. Examples of alkenyl include but are not limited to —CH₂—CH═CH—CH₃ and —CH₂—CH₂-cyclohexenyl, where the ethyl group of the later example can be attached to the cyclohexenyl moiety at any available position on the ring.

“Alkynyl” refers to an unsaturated hydrocarbon group having at least one site of acetylenic unsaturation (i.e., having at least one moiety of the formula CC) and preferably having from 2 to 10 carbon atoms and more preferably 3 to 8 carbon atoms.

“Substituted alkyl” refers to an alkyl group having from 1 to 5 substituents including, but not limited to, substituents such as alkoxy, substituted alkoxy, acyl, acyloxy, carbonylalkoxy, acylamino, substituted or unsubstituted amino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, aryl, substituted aryl, heteroaryl, substituted heteroaryl, aryloxy, substituted aryloxy, cyano, halo, hydroxyl, nitro, carboxyl, thiol, thioalkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aralkyl, aminosulfonyl, sulfonylamino, sulfonyl, oxo, carbonylalkylenealkoxy and the like.

“Substituted alkenyl” refers to alkenyl group having from 1 to 5 substituents s including, but not limited to, substituents such as alkoxy, substituted alkoxy, acyl, acyloxy, carbonylalkoxy, acylamino, substituted or unsubstituted amino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, aryl, substituted aryl, heteroaryl, substituted heteroaryl, aryloxy, substituted aryloxy, cyano, halo, hydroxyl, nitro, carboxyl, thiol, thioalkyl, substituted or unsubstituted alkyl, substituted or unsubstituted alkynyl, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aralkyl, aminosulfonyl, sulfonylamino, sulfonyl, oxo, carbonylalkylenealkoxy and the like.

“Substituted alkynyl” refers to alkynyl groups having from 1 to 5 substituents including, but not limited to, groups such as alkoxy, substituted alkoxy, acyl, acyloxy, carbonylalkoxy, acylamino, substituted or unsubstituted amino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, aryl, substituted aryl, heteroaryl, substituted heteroaryl, aryloxy, substituted aryloxy, cyano, halo, hydroxyl, nitro, carboxyl, thiol, thioalkyl, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aralkyl, aminosulfonyl, sulfonylamino, sulfonyl, oxo, carbonylalkylenealkoxy and the like.

“Acyl” refers to the groups H—C(O)—, alkyl-C(O)—, substituted alkyl-C(O)—, alkenyl-C(O)—, substituted alkenyl-C(O)—, alkynyl-C(O)—, substituted alkynyl-C(O)—, aryl-C(O)—, substituted aryl-C(O)—, heteroaryl-C(O)—, substituted heteroaryl-C(O)—, heterocyclic-C(O)—, and substituted heterocyclic-C(O)—, wherein alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic and substituted heterocyclic are as defined herein.

“Acyloxy” refers to the groups H—C(O)O—, alkyl-C(O)O—, substituted alkyl-C(O)O—, alkenyl-C(O)O—, substituted alkenyl-C(O)O—, alkynyl-C(O)O—, substituted alkynyl-C(O)O—, aryl-C(O)O—, substituted aryl-C(O)O—, heteroaryl-C(O)O—, substituted heteroaryl-C(O)O—, heterocyclic-C(O)O—, and substituted heterocyclic-C(O)O—, wherein alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic and substituted heterocyclic are as defined herein.

“Heterocycle”, “heterocyclic”, or “heterocyclyl” refers to a saturated or an unsaturated non-aromatic group having a single ring or multiple condensed rings, and having from 1 to 10 annular carbon atoms and from 1 to 4 annular heteroatoms, such as nitrogen, sulfur or oxygen. A heterocycle comprising more than one ring may be fused, spiro or bridged, or any combination thereof. In fused ring systems, one or more of the rings can be aryl or heteroaryl. A heterocycle having more than one ring where at least one ring is aromatic may be connected to the parent structure at either a non-aromatic ring position or at an aromatic ring position. In one variation, a heterocycle having more than one ring where at least one ring is aromatic is connected to the parent structure at a non-aromatic ring position.

“Substituted heterocyclic” or “substituted heterocyclyl” refers to a heterocycle group which is substituted with from 1 to 3 substituents including, but not limited to, substituents such as alkoxy, substituted alkoxy, acyl, acyloxy, carbonylalkoxy, acylamino, substituted or unsubstituted amino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, aryl, substituted aryl, heteroaryl, substituted heteroaryl, aryloxy, substituted aryloxy, cyano, halo, hydroxyl, nitro, carboxyl, thiol, thioalkyl, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted aralkyl, aminosulfonyl, sulfonylamino, sulfonyl, oxo, carbonylalkylenealkoxy and the like. In one variation, a substituted heterocycle is a heterocycle substituted with an additional ring, wherein the additional ring may be aromatic or non-aromatic.

“Aryl” or “Ar” refers to an unsaturated aromatic carbocyclic group having a single ring (e.g., phenyl) or multiple condensed rings (e.g., naphthyl or anthryl) which condensed rings may or may not be aromatic. In one variation, the aryl group contains from 6 to 14 annular carbon atoms. An aryl group having more than one ring where at least one ring is non-aromatic may be connected to the parent structure at either an aromatic ring position or at a non-aromatic ring position. In one variation, an aryl group having more than one ring where at least one ring is non-aromatic is connected to the parent structure at an aromatic ring position.

“Heteroaryl” or “HetAr” refers to an unsaturated aromatic carbocyclic group having from 2 to 10 annular carbon atoms and at least one annular heteroatom, including but not limited to heteroatoms such as nitrogen, oxygen and sulfur. A heteroaryl group may have a single ring (e.g., pyridyl, furyl) or multiple condensed rings (e.g., indolizinyl, benzothienyl) which condensed rings may or may not be aromatic. A heteroaryl group having more than one ring where at least one ring is non-aromatic may be connected to the parent structure at either an aromatic ring position or at a non-aromatic ring position. In one variation, a heteroaryl group having more than one ring where at least one ring is non-aromatic is connected to the parent structure at an aromatic ring position.

“Substituted aryl” refers to an aryl group having 1 to 5 substituents including, but not limited to, groups such as alkoxy, substituted alkoxy, acyl, acyloxy, carbonylalkoxy, acylamino, substituted or unsubstituted amino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, heteroaryl, substituted heteroaryl, aryloxy, substituted aryloxy, cyano, halo, hydroxyl, nitro, carboxyl, thiol, thioalkyl, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aralkyl, aminosulfonyl, sulfonylamino, sulfonyl, oxo, carbonylalkylenealkoxy and the like.

“Substituted heteroaryl” refers to a heteroaryl group having 1 to 5 substituents including, but not limited to, groups such as alkoxy, substituted alkoxy, acyl, acyloxy, carbonylalkoxy, acylamino, substituted or unsubstituted amino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, aryl, substituted aryl, aryloxy, substituted aryloxy, cyano, halo, hydroxyl, nitro, carboxyl, thiol, thioalkyl, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aralkyl, aminosulfonyl, sulfonylamino, sulfonyl, oxo, carbonylalkylenealkoxy and the like.

“Aralkyl” refers to a residue in which an aryl moiety is attached to an alkyl residue and wherein the aralkyl group may be attached to the parent structure at either the aryl or the alkyl residue. Preferably, an aralkyl is connected to the parent structure via the alkyl moiety. A “substituted aralkyl” refers to a residue in which an aryl moiety is attached to a substituted alkyl residue and wherein the aralkyl group may be attached to the parent structure at either the aryl or the alkyl residue. When an aralkyl is connected to the parent structure via the alkyl moiety, it may also be referred to as an “alkaryl”. More particular alkaryl groups are those having 1 to 3 carbon atoms in the alkyl moiety (a “C₁-C₃ alkaryl”).

“Alkoxy” refers to the group alkyl-O—, which includes, by way of example, methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, tert-butoxy, sec-butoxy, n-pentoxy, n-hexoxy, 1,2-dimethylbutoxy, and the like. Similarly, alkenyloxy refers to the group “alkenyl-O—” and alkynyloxy refers to the group “alkynyl-O—”. “Substituted alkoxy” refers to the group substituted alkyl-O.

“Unsubstituted amino” refers to the group —NH₂.

“Substituted amino” refers to the group —NR_(a)R_(b), where either (a) each R_(a) and R_(b) group is independently selected from the group consisting of H, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic, substituted heterocyclic, provided that both R_(a) and R_(b) groups are not H; or (b) R_(a) and R_(b) are joined together with the nitrogen atom to form a heterocyclic or substituted heterocyclic ring.

“Acylamino” refers to the group —C(O)NR_(a)R_(b) where R_(a) and R_(b) are independently selected from the group consisting of H, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic and substituted heterocyclic, or R_(a) and R_(b) groups can be joined together with the nitrogen atom to form a heterocyclic or substituted heterocyclic ring.

“Acyclic acylamino” refers to the group —C(O)NR_(a)R_(b) where R_(a) and R_(b) are independently selected from the group consisting of H, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic, substituted heterocyclic.

“Cyclic acylamino” refers to the group —C(O)NR_(a)R_(b) where R_(a) and R_(b) groups are joined together with the nitrogen atom to form a heterocyclic or substituted heterocyclic ring. Examples of cyclic acylamino group include but are not limited to —C(O)(1-piperidinyl), —C(O)(1-piperazinyl), —C(O)(4-methyl-1-piperazinyl) and —C(O)(1-pyrrolidinyl).

“Aminocarbonylalkoxy” refers to the group —NR_(a)C(O)OR_(b) where each R_(a) and R_(b) group is independently selected from the group consisting of H, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic and substituted heterocyclyl.

“Aminoacyl” refers to the group —NR_(a)C(O)R_(b) where each R_(a) and R_(b) group is independently selected from the group consisting of H, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic and substituted heterocyclic. Preferably, R_(a) is H or alkyl.

“Aminosulfonyl” refers to the groups —NRSO₂-alkyl, —NRSO₂ substituted alkyl, —NRSO₂-alkenyl, —NRSO₂-substituted alkenyl, —NRSO₂-alkynyl, —NRSO₂-substituted alkynyl, —NRSO₂-aryl, —NRSO₂-substituted aryl, —NRSO₂-heteroaryl, —NRSO₂-substituted heteroaryl, —NRSO₂-heterocyclic, and —NRSO₂-substituted heterocyclic, where R is H or alkyl and wherein alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic and substituted heterocyclic are as defined herein.

“Sulfonylamino” refers to the groups —SO₂NH₂, —SO₂NR-alkyl, —SO₂NR-substituted alkyl, —SO₂NR-alkenyl, —SO₂NR-substituted alkenyl, —SO₂NR-alkynyl, —SO₂NR-substituted alkynyl, —SO₂NR-aryl, —SO₂NR-substituted aryl, —SO₂NR-heteroaryl, —SO₂NR-substituted heteroaryl, —SO₂NR-heterocyclic, and —SO₂NR-substituted heterocyclic, where R is H or alkyl, or —SO₂NR₂, where the two R groups are taken together and with the nitrogen atom to which they are attached to form a heterocyclic or substituted heterocyclic ring.

“Sulfonyl” refers to the groups —SO₂-alkyl, —SO₂-substituted alkyl, —SO₂-alkenyl, —SO₂-substituted alkenyl, —SO₂-alkynyl, —SO₂-substituted alkynyl, —SO₂-aryl, —SO₂-substituted aryl, —SO₂-heteroaryl, —SO₂-substituted heteroaryl, —SO₂-heterocyclic, and —SO₂-substituted heterocyclic.

“Carbonylalkylenealkoxy” refers to the group —C(═O)—(CH₂)_(n)—OR where R is a substituted or unsubstituted alkyl and n is an integer from 1 to 100, more preferably n is an integer from 1 to 10 or 1 to 5.

“Halo” or “halogen” refers to elements of the Group 17 series having atomic number 9 to 85. Preferred halo groups include the radicals of fluorine, chlorine, bromine and iodine. Where a residue is substituted with more than one halogen, it may be referred to by using a prefix corresponding to the number of halogen moieties attached, e.g., dihaloaryl, dihaloalkyl, trihaloaryl etc. refer to aryl and alkyl substituted with two (“di”) or three (“tri”) halo groups, which may be but are not necessarily the same halogen; thus 4-chloro-3-fluorophenyl is within the scope of dihaloaryl. An alkyl group in which each H is replaced with a halo group is referred to as a “perhaloalkyl.” A preferred perhaloalkyl group is trifluoroalkyl (—CF₃). Similarly, “perhaloalkoxy” refers to an alkoxy group in which a halogen takes the place of each H in the hydrocarbon making up the alkyl moiety of the alkoxy group. An example of a perhaloalkoxy group is trifluoromethoxy (—OCF₃).

“Carbonyl” refers to the group C═O.

“Cyano” refers to the group —CN.

“Oxo” refers to the moiety ═O.

“Nitro” refers to the group —NO₂.

“Thioalkyl” refers to the groups —S-alkyl.

“Alkylsulfonylamino” refers to the groups —R¹SO₂NR_(a)R_(b) where R_(a) and R_(b) are independently selected from the group consisting of H, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic, substituted heterocyclic, or the R_(a) and R_(b) groups can be joined together with the nitrogen atom to form a heterocyclic or substituted heterocyclic ring and R¹ is an alkyl group.

“Carbonylalkoxy” refers to as used herein refers to the groups —C(O)O-alkyl, —C(O)O— substituted alkyl, —C(O)O-aryl, —C(O)O-substituted aryl, —C(O)O-alkenyl, —C(O)O-substituted alkenyl, —C(O)O-alkynyl, —C(O)O-substituted alkynyl, —C(O)O-heteroaryl, —C(O)O-substituted heteroaryl, —C(O)O-heterocyclic or —C(O)O-substituted heterocyclic.

“Geminal” refers to the relationship between two moieties that are attached to the same atom. For example, in the residue —CH₂—CHR¹R², R¹ and R² are geminal and R¹ may be referred to as a geminal R group to R².

“Vicinal” refers to the relationship between two moieties that are attached to adjacent atoms. For example, in the residue —CHR¹—CH₂R², R¹ and R² are vicinal and R¹ may be referred to as a vicinal R group to R².

A composition of “substantially pure” compound means that the composition contains no more than 15% or preferably no more than 10% or more preferably no more than 5% or even more preferably no more than 3% and most preferably no more than 1% impurity, which impurity may be the compound in a different stereochemical form. For instance, a composition of substantially pure S compound means that the composition contains no more than 15% or no more than 10% or no more than 5% or no more than 3% or no more than 1% of the R form of the compound.

Compounds of the Invention

Compounds according to the invention are detailed herein, including in the Brief Summary of the Invention and the appended claims. Thus, compounds of the invention include any compounds detailed herein. The invention includes the use of all of the compounds described herein, including any and all stereoisomers, salts and solvates of the compounds described as histamine receptor modulators. Further methods of using the compounds of the invention are detailed throughout.

The invention embraces compounds of the formula (I):

where:

R¹ is H, hydroxyl, nitro, cyano, halo, substituted or unsubstituted C₁-C₈ alkyl, substituted or unsubstituted C₂-C₈ alkenyl, substituted or unsubstituted C₂-C₈ alkynyl, perhaloalkyl, acyl, acyloxy, carbonylalkoxy, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted aralkyl, C₁-C₈ perhaloalkoxy, alkoxy, aryloxy, carboxyl, thiol, thioalkyl, substituted or unsubstituted amino, acylamino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, aminosulfonyl, sulfonylamino, sulfonyl or carbonylalkylenealkoxy;

each R^(2a) and R^(2b) is independently H, substituted or unsubstituted C₁-C₈ alkyl, halo, hydroxyl, alkoxy, cyano, nitro or R^(2a) and R^(2b) are taken together to form a carbonyl moiety;

each R^(3a) and R^(3b) is independently H, substituted or unsubstituted C₁-C₈ alkyl, halo, cyano or nitro or R^(3a) and R^(3b) are taken together to form a carbonyl moiety;

each X⁷, X⁸, X⁹ and X¹⁰ is independently N or CR⁴;

m and q are independently 0 or 1;

X¹ is N or CH;

each R⁴ is independently H, hydroxyl, nitro, cyano, halo, C₁-C₈ perhaloalkyl, substituted or unsubstituted C₁-C₈ alkyl, substituted or unsubstituted C₂-C₈ alkenyl, substituted or unsubstituted C₂-C₈ alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, C₁-C₈ perhaloalkoxy, C₁-C₈ alkoxy, aryloxy, carboxyl, thiol, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aralkyl, thioalkyl, substituted or unsubstituted amino, acylamino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, aminosulfonyl, sulfonylamino, sulfonyl, carbonylalkylenealkoxy, alkylsulfonylamino or acyl;

each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is independently H, hydroxyl, C₁-C₈ alkyl or is taken together with the carbon to which it is attached and a geminal R^(8(e-f)) to form a cycloalkyl moiety;

each R^(10a) and R^(10b) is independently H, halo, a substituted or unsubstituted C₁-C₈ alkyl, hydroxyl, alkoxyl or R^(10a) and R^(10b) are taken together to form a carbonyl;

Q is acylamino, carbonylalkoxy, acyloxy, aminoacyl or aminocarbonylalkoxy; provided that the compound is other than a compound according to proviso 1 and proviso 2. In one variation, the compound is of the formula (I) provided that the compound is other than any of compounds 1x-6x and a compound of proviso 2. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of Formula (I), including those listed in proviso 1 or proviso 2 or a salt thereof. In one variation, the compound is of the formula (I) provided that the compound is other than a compound of the formula (X):

wherein:

-   -   R_(5c) is selected from alkyl, substituted alkyl, and aralkyl;     -   R_(5b) is selected from alkyl, aryl, and substituted aryl;     -   R_(5a) is alkyl; and     -   R_(5d) is alkyl.         In another variation, the compound is of the formula (I) and         includes compounds of the formula (X).

In another variation, the invention embraces compounds of the formula (A):

wherein X⁷, X⁸, X⁹ and X¹⁰; R¹; R^(2a), R^(2b), R^(3a), R^(3b); R⁴, R^(8a), R^(8b), R^(8c), R^(8d), R^(8e), R^(8f), R^(10a) and R^(10b); and m and q are as defined in formula (I), provided that the compound is other than a compound in Table 1, or a salt thereof. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (A), including those listed in Table 1 or a salt thereof. In another variation, the invention embraces compounds of the formula (A) provided that at least one of X⁷, X⁸, X⁹ and X¹⁰ is other than CH. In another variation, the invention embraces compounds of the formula (A) where X⁹ is other than CR⁴ where R⁴ is H, 4-methyl-1-piperidinylcarbonyl or formyl group.

The invention also embraces compounds of the formula (B):

wherein X⁷, X⁸, X⁹ and X¹⁰; R¹; R^(2a), R^(2b), R^(3a), R^(3b), R⁴, R^(8c), R^(8d), R^(8e), R^(8f), R^(10a) and R^(10b) are as defined in formula (I), provided that the compound is other than any of compounds 7x, 10x, 63x, 64x, 65x, 66x, 67x, 68x, 69x, 70x, 71x, 72x, 73x, 74x, 75x, 76x, 77x, 78x, 79x, 80x, 81x, 82x, 83x, 84x, 85x, 86x, 87x, 88x, 89x, 90x, 91x, 92x, 93x, 94x, 95x, 96x, 97x, 98x, 99x, 100x, 101x, 102x, 103x, 104x, 105x and 106x, or a salt thereof. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (B), including compounds 7x, 10x, 63x, 64x, 65x, 66x, 67x, 68x, 69x, 70x, 71x, 72x, 73x, 74x, 75x, 76x, 77x, 78x, 79x, 80x, 81x, 82x, 83x, 84x, 85x, 86x, 87x, 88x, 89x, 90x, 91x, 92x, 93x, 94x, 95x, 96x, 97x, 98x, 99x, 100x, 101x, 102x, 103x, 104x, 105x or 106x or a salt thereof.

The invention also embraces compounds of the formula (C):

wherein X⁷, X⁸, X⁹ and X¹⁰, R¹, R^(2a), R^(2b), R^(3a), R^(3b), R⁴, R^(8a), R^(8b), R^(8c), R^(8d), R^(8e), R^(8f), R^(10a) and R^(10b) are as defined in formula (I) or a salt thereof.

In one variation, the compound is of the formula (C) where one of X⁷, X⁸, X⁹ and X¹⁰ is N. In one such variation, X⁹ is N and X⁷, X⁸ and X¹⁰ are CH. In one variation, the compound is of the formula (C) where X⁹ is N, X⁷, X⁸ and X¹⁰ are CH and R¹ is alkyl e.g. methyl. In another variation, the compound is of the formula (C) where X⁹ is N, R¹ is alkyl and Q is carbonylalkoxy, acylamino or aminoacyl. In yet another variation, the compound is of the formula (C) where X⁷, X⁸ and X¹⁰ are CH, X⁹ is N, R¹ is alkyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H and Q is carbonylalkoxy, acylamino or aminoacyl. In one specific variation, the compound is of the formula (C) where X⁷, X⁸ and X¹⁰ are CH, X⁹ is N, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a), R^(10b), R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H and Q is carbonylalkoxy, acylamino or aminoacyl. In one such specific variation, Q is acylamino, e.g. —C(O)NHR′ where R′ is substituted or unsubstituted alkyl or cycloalkyl.

In one variation, the compound is of the formula (C) where each of X⁷, X⁸, X⁹ and X¹⁰ is CR⁴ where R⁴ is as defined in formula (I) or any variation thereof. In one such variation, X⁷, X⁸ and X¹⁰ are CH and X⁹ is CR⁴ where R⁴ is alkyl. In another variation, the compound is of the formula (C) where X⁷, X⁸ and X¹⁰ are CH, X⁹ is CR⁴ where R⁴ is alkyl and R¹ is alkyl. In yet another variation, the compound is of the formula (C) where X⁷, X⁸ and X¹⁰ are CH, X⁹ is CR⁴ where R⁴ is alkyl, R¹ is alkyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H and Q is acylamino or carbonylalkoxy.

In one specific variation, the compound is of the formula (C) where X⁷, X⁸ and X¹⁰ are CH and X⁹ is CR⁴ where R⁴ is methyl, R¹ is methyl, each R^(2a), R^(2b), R^(3b), R^(10a), R^(10b), R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H and Q is acylamino or carbonylalkoxy. In one such specific variation, Q is acylamino, e.g. —C(O)NHR′ where R′ is substituted or unsubstituted alkyl.

The invention also embraces compounds of the formula (D):

wherein X⁷, X⁸, X⁹ and X¹⁰; R¹, R^(2a), R^(2b), R^(3a), R^(3b), R⁴, R^(8e), R^(8f), R^(10a) and R^(10b) are as defined in formula (I), provided that the compound is other than any of compounds 1x, 2x, 3x, 4x, 5x, 6x, 8x, 9x, 11x, 12x, 13x, 14x, 15x, 16x, 17x, 18x, 19x, 20x, 21x, 22x, 23x, 24x, 25x, 26x, 27x, 28x, 29x, 30x, 31x, 32x, 33x, 34x, 35x, 36x, 37x, 38x, 39x, 40x, 41x, 42x, 43x, 44x, 45x, 46x, 47x, 48x, 49x, 50x, 51x, 52x, 53x, 54x, 55x, 56x, 57x, 58x, 59x, 60x, 61x, 62x, 107x, 108x, 109x and 110x, or a salt thereof. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (D), including compounds 1x, 2x, 3x, 4x, 5x, 6x, 8x, 9x, 11x, 12x, 13x, 14x, 15x, 16x, 17x, 18x, 19x, 20x, 21x, 22x, 23x, 24x, 25x, 26x, 27x, 28x, 29x, 30x, 31x, 32x, 33x, 34x, 35x, 36x, 37x, 38x, 39x, 40x, 41x, 42x, 43x, 44x, 45x, 46x, 47x, 48x, 49x, 50x, 51x, 52x, 53x, 54x, 55x, 56x, 57x, 58x, 59x, 60x, 61x, 62x, 107x, 108x, 109x or 110x or a salt thereof.

In one variation, a compound of the invention is of the formula (I) where: R¹ is a substituted or unsubstituted C₁-C₈ alkyl, acyl, acyloxy, carbonylalkoxy, substituted or unsubstituted heterocyclyl or substituted or unsubstituted aryl; each R^(2a) and R^(2b) is independently H, methyl, fluoro or R^(2a) and R^(2b) are taken together to form a carbonyl moiety; each R^(3a) and R^(3b) is independently H or fluoro; and each R^(10a) and R^(10b) is independently H, halo, hydroxyl or methyl or R^(10a) and R^(10b) are taken together to form a carbonyl. This variation of formula (I) is referred to herein as formula “(Ia)”. All variations referring to formula (I), where applicable, may apply equally to any of formula (A)-(D) the same as if each and every variation were specifically and individually listed.

In a particular embodiment, the compound is of the formula (I) or (Ia) where X⁷, X⁸, X⁹ and X¹⁰ are CR⁴. In another embodiment, the compound is of the formula (I) or (Ia) where at least one of X⁷, X⁸, X⁹ and X¹⁰ is N. Another variation provides a compound of the formula (I) or (Ia) where at least two of X⁷, X⁸, X⁹ and X¹⁰ are N. A further variation provides a compound of the formula (I) or (Ia) where 2 of X⁷, X⁸, X⁹ and X¹⁰ are N and 2 of X⁷, X⁸, X⁹ and X¹⁰ are CR⁴. A compound of the formula (I) or (Ia) where 1 of X⁷, X⁸, X⁹ and X¹⁰ is N and 3 of X⁷, X⁸, X⁹ and X¹⁰ are CR⁴ is also embraced by this invention.

The invention further embraces compounds of the formula (E):

where:

R¹ is H, hydroxyl, nitro, cyano, halo, substituted or unsubstituted C₁-C₈ alkyl, substituted or unsubstituted C₂-C₈ alkenyl, substituted or unsubstituted C₂-C₈ alkynyl, perhaloalkyl, acyl, acyloxy, carbonylalkoxy, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted aralkyl, C₁-C₈ perhaloalkoxy, alkoxy, aryloxy, carboxyl, thiol, thioalkyl, substituted or unsubstituted amino, acylamino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, aminosulfonyl, sulfonylamino, sulfonyl or carbonylalkylenealkoxy;

each R^(2a) and R^(2b) is independently H, substituted or unsubstituted C₁-C₈ alkyl, halo, cyano, hydroxyl, alkoxy, nitro or R^(2a) and R^(2b) are taken together with the carbon to which they are attached to form a cycloalkyl moiety or a carbonyl moiety;

each R^(3a) and R^(3b) is independently H, substituted or unsubstituted C₁-C₈ alkyl, halo, cyano hydroxyl, alkoxy, nitro or R^(3a) and R^(3b) are taken together with the carbon to which they are attached to form a cycloalkyl moiety or a carbonyl moiety;

each X⁷, X⁸, X⁹ and X¹⁰ is independently N or CR⁴;

m and q are independently 0 or 1;

n is 0 or 1;

each R⁴ is independently H, hydroxyl, nitro, cyano, halo, C₁-C₈ perhaloalkyl, substituted or unsubstituted C₁-C₈ alkyl, substituted or unsubstituted C₂-C₈ alkenyl, substituted or unsubstituted C₂-C₈ alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, C₁-C₈ perhaloalkoxy, C₁-C₈ alkoxy, aryloxy, carboxyl, thiol, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aralkyl, thioalkyl, substituted or unsubstituted amino, acylamino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, aminosulfonyl, sulfonylamino, sulfonyl, carbonylalkylenealkoxy, alkylsulfonylamino or acyl;

each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is independently H, hydroxyl, substituted or unsubstituted alkyl or is taken together with the carbon to which it is attached and a geminal R^(8(a-f)) to form a cycloalkyl moiety;

each R^(10a) and R^(10b) is independently H, substituted or unsubstituted C₁-C₈ alkyl, halo, hydroxyl, alkoxyl or R^(10a) and R^(10b) are taken together with the carbon to which they are attached to form a cycloalkyl moiety or a carbonyl moiety; and

Q is acyclic or cyclic acylamino, carbonylalkoxy, acyloxy, aminoacyl, aminocarbonylalkoxy, substituted or unsubstituted lactam or substituted or unsubstituted cycloalkyl;

provided that: (ia) Q is substituted or unsubstituted cycloalkyl or a lactam moiety when each of m, n and q is 0 and (ib) m, n and q are 0 when Q is a substituted or unsubstituted cycloalkyl or a lactam moiety, (ii) Q is cyclic acylamino only when each of m, n and q is 1, (iii) when Q is carbonylalkoxy, each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is other than cycloalkyl and substituted alkyl; (iv) the compound is other than a compound in Table 1, and (v) the compound is other than 5-cyclohexyl-2,3,4,5-tetrahydro-2-methyl-1H-pyrido[4,3-b]indole and 5-cyclopentyl-2,3,4,5-tetrahydro-2-[(4-methyl-1H-imidazol-5-yl)methyl]-1H-pyrido[4,3-b]indol-1-one;

or a salt thereof. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (E), including those listed in Table 1,5-cyclohexyl-2,3,4,5-tetrahydro-2-methyl-1H-pyrido[4,3-b]indole or 5-cyclopentyl-2,3,4,5-tetrahydro-2-[(4-methyl-1H-imidazol-5-yl)methyl]-1H-pyrido[4,3-b]indol-1-one or a salt thereof.

In one variation, the compound is of the formula (E) where X⁹ is N provided that the compound is other than compounds 109x and 110x. In another variation, the compound is of the formula (E) where X⁹ is N and R¹ is a substituted alkyl or unsubstituted alkyl other than isopropyl. In another variation, the compound is of the formula (E) where X⁹ is N and R¹ is methyl. In one variation, the compound is of the formula (E) where X⁹ is N, n is 1 and at least one of m and q are 1. In another variation, the compound is of the formula (E) where X⁹ is N and Q is other than acylamino. In yet another variation, the compound is of the formula (E) where X⁹ is N and Q is aminoacyl, carbonylalkoxy or acyloxy. In one variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is N and R¹ is methyl. In another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is N, R¹ is methyl and each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H. In another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is N, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H and each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H when present. In another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is N, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, each m, n and q is 1 and each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H. In yet another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is N, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, q is 0, m and n are 1 and each R^(8c), R^(8d), R^(8e) and R^(8f) is H. In one particular variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is N, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H when present and Q is acyclic acylamino, aminoacyl or carbonylalkoxy.

In one variation, the compound is of the formula (E) where X⁹ is CR⁴ where R⁴ is chloro.

In another variation, the compound is of the formula (E) where X⁹ is CR⁴ where R⁴ is chloro and n is 1. In another variation, the compound is of the formula (E) where X⁹ is CR⁴ where R⁴ is chloro, n is 1 and one of m and q is 1 and the other is 0. In yet another variation, the compound is of the formula (E) where X⁹ is CR⁴ where R⁴ is chloro, n is 1 and m and q are 0. In one variation, the compound is of the formula (E) where X⁹ is CR⁴ where R⁴ is chloro and R¹ is alkyl, e.g. methyl. In another variation, the compound is of the formula (E) where X⁹ is CR⁴ where R⁴ is chloro and Q is acylamino or carbonylalkoxy. In one variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is CR⁴ where R⁴ is halo, R¹ is methyl and Q is other than ethoxycarbonyl. In another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is CR⁴ where R⁴ is halo, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H and Q is other than ethoxycarbonyl. In another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is CR⁴ where R⁴ is halo, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H when present and Q is other than ethoxycarbonyl. In another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is CR⁴ where R⁴ is halo, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, q is 0, m and n are 1, each R^(8c), R^(8d), R^(8e) and R^(8f) is H and Q is other than ethoxycarbonyl. In yet another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is CR⁴ where R⁴ is halo, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H when present and Q is acyclic acylamino or aminoacyl. In one variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is CR⁴ where R⁴ is chloro and R¹ is alkyl. In another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is CR⁴ where R⁴ is chloro, R¹ is alkyl and each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H. In another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is CR⁴ where R⁴ is chloro, R¹ is alkyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H and each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H when present. In another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is CR⁴ where R⁴ is chloro, R¹ is alkyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, each m, n and q is 1 and each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H. In yet another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is CR⁴ where R⁴ is chloro, R¹ is alkyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, q is 0, m and n are 1 and each R^(8c), R^(8d), R^(8e) and R^(8f) is H. In one particular variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is CR⁴ where R⁴ is chloro, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H when present and Q is acyclic acylamino, aminoacyl or carbonylalkoxy.

In one variation, the compound is of the formula (E) where X⁹ is CR⁴ where R⁴ is alkyl and each n, m and q is 1. In another variation, the compound is of the formula (E) where X⁹ is CR⁴ where R⁴ is alkyl and R¹ is alkyl provided that the compound is other than any of compounds 13x, 20x and 73x. In another variation, the compound is of the formula (E) where X⁹ is CR⁴ where R⁴ is alkyl, R¹ is methyl and Q is other than —C(O)OCH₂CH₃. In one variation, the compound is of the formula (E) where X⁹ is CR⁴ where R⁴ is alkyl and Q is substituted acylamino. In another variation, the compound is of the formula (E) where X⁹ is CR⁴ where R⁴ is alkyl, Q is acyclic acylamino and R¹ is a substituted alkyl or unsubstituted alkyl other than isopropyl. In yet another variation, the compound is of the formula (E) where X⁹ is CR⁴ where R⁴ is alkyl, R¹ is methyl and Q is acyclic acylamino, aminoacyl or aminocarbonylalkoxy. In one variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is CR⁴ where R⁴ is alkyl, R¹ is methyl and Q is other than ethoxycarbonyl. In another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is CR⁴ where R⁴ is alkyl, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H and Q is other than ethoxycarbonyl. In another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is CR⁴ where R⁴ is alkyl, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H when present and Q is other than ethoxycarbonyl. In another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is CR⁴ where R⁴ is alkyl, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, q is 0, m and n are 1, each R^(8c), R^(8d), R^(8e) and R^(8f) is H and Q is other than ethoxycarbonyl. In yet another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is CR⁴ where R⁴ is alkyl, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H when present and Q is acyclic acylamino or aminoacyl. In one particular variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is CR⁴ where R⁴ is methyl, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H when present and Q is acyclic acylamino or aminoacyl.

In one variation, the compound is of the formula (E) where R¹ is a substituted alkyl or unsubstituted alkyl other than isopropyl and Q is acyclic acylamino other than —C(O)NMe₂ and —C(O)NH₂. In another variation, the compound is of the formula (E) where R¹ is a substituted alkyl or unsubstituted alkyl other than isopropyl and Q is acylamino of the formula —C(O)NHR′ where R′ is other than H. In yet another variation, the compound is of the formula (E) where R¹ is methyl and Q is acylamino of the formula —C(O)NHR′ where R′ is unsubstituted or substituted alkyl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted aryl, unsubstituted or substituted heteroaryl or unsubstituted or substituted heterocyclyl. In one variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is N or CR⁴ where R⁴ is chloro or methyl, R¹ is methyl and Q is acyclic acylamino. In another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is N or CR⁴ where R⁴ is chloro or methyl, R¹ is methyl, each R^(2a), R^(2b). R^(3a), R^(3b), R^(10a) and R^(10b) is H and Q is acyclic acylamino. In another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is N or CR⁴ where R⁴ is chloro or methyl, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H when present and Q is acyclic acylamino. In one particular variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is N or CR⁴ where R⁴ is chloro or methyl, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H when present and Q is acylamino of the formula —C(O)NHR′ where R′ is unsubstituted or substituted alkyl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted aryl, unsubstituted or substituted heteroaryl or unsubstituted or substituted heterocyclyl.

In one variation, the compound is of the formula (E) where Q is aminoacyl. In another variation, the compound is of the formula (E) where Q is aminocarbonylalkoxy. In one variation, the compound is of the formula (E) where Q is acylamino of the formula —C(O)NHR′ where R′ is unsubstituted or substituted alkyl, substituted cycloalkyl, unsubstituted or substituted aryl, unsubstituted or substituted heteroaryl or unsubstituted or substituted heterocyclyl. In another variation, the compound is of the formula (E) where Q is carbonylalkoxy other than —C(O)OCH₂CH₃. In yet another variation, the compound is of the formula (E) where Q is carbonylalkoxy of the formula —C(O)OR′ where R′ is unsubstituted C₃-C₈ alkyl, substituted alkyl, unsubstituted or substituted aryl, unsubstituted or substituted heteroaryl or unsubstituted or substituted heterocyclyl. In one variation, the compound is of the formula (E) where Q is —C(O)NH₂, R¹ is methyl and at least one of X⁷, X⁸, X⁹ and X¹⁰ is other than CH. In another variation, the compound is of the formula (E) where Q is —C(O)NMe₂ and R¹ is methyl. In another variation, the compound is of the formula (E) where Q is —C(O)NMe₂ and at least one of X⁷, X⁸, X⁹ and X¹⁰ is CR⁴ where R⁴ is halo or alkyl. In one variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is N or CR⁴ where R⁴ is chloro or methyl, R¹ is methyl and Q is aminoacyl or aminocarbonylalkoxy. In another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is N or CR⁴ where R⁴ is chloro or methyl, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H and Q is aminoacyl or aminocarbonylalkoxy. In another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is N or CR⁴ where R⁴ is chloro or methyl, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H when present and Q is aminoacyl or aminocarbonylalkoxy. In another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is N or CR⁴ where R⁴ is methyl, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H when present and Q is aminoacyl or aminocarbonylalkoxy. In yet another variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is N or CR⁴ where R⁴ is methyl, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H when present and Q is aminoacyl of the formula —NHC(O)R′ where R′ is H, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclyl or substituted heterocyclyl. In a particular variation, the compound is of the formula (E) where each X⁷, X⁸ and X¹⁰ is CH, X⁹ is N or CR⁴ where R⁴ is methyl, R¹ is methyl, each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H when present and Q is of the formula —NHC(O)R′ where R′ is alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclyl, substituted heterocyclyl, alkoxy or substituted alkoxy.

In one variation, the invention embraces the compound of formula (F):

or a salt thereof, where R¹, X⁷, X⁸, X⁹, X¹⁰, R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) and R⁴ are as defined in formula (E) or any applicable variation thereof and Q is substituted or unsubstituted cycloalkyl or a lactam moiety, provided that the compound is other than any of 5-cyclohexyl-2,3,4,5-tetrahydro-2-methyl-1H-pyrido[4,3-b]indole and 5-cyclopentyl-2,3,4,5-tetrahydro-2-[(4-methyl-1H-imidazol-5-yl)methyl]-1H-pyrido[4,3-b]indol-1-one. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (F), including 5-cyclohexyl-2,3,4,5-tetrahydro-2-methyl-1H-pyrido[4,3-b]indole and 5-cyclopentyl-2,3,4,5-tetrahydro-2-[(4-methyl-1H-imidazol-5-yl)methyl]-1H-pyrido[4,3-b]indol-1-one or a salt thereof.

In one variation, the compound is of the formula (F) where Q is substituted cycloalkyl or a lactam moiety. The lactam moiety may be a substituted or unsubstituted lastam moiety. When the lactam is substituted, in one variation, the substituent is attached to the nitrogen of the lactam ring (e.g. N-methyl lactam). In another variation, the compound is of the formula (F) where at least one of X⁷, X⁸, X⁹ and X¹⁰ is other than CH. In another variation, the compound is of the formula (F) where Q is a moiety selected from the structures:

In another variation, a compound of the invention is of the formula (I) or (Ia) where X⁷, X⁸, X⁹ and X¹⁰ are taken together to provide an aromatic moiety selected from the following structures:

where each R⁴ is as defined for formula (I) or (Ia); or in a particular variation, where each R⁴ is independently hydroxyl, halo, C₁-C₈ perhaloalkyl, substituted or unsubstituted C₁-C₈ alkyl, substituted or unsubstituted C₂-C₈ alkenyl, substituted or unsubstituted C₂-C₈ alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, C₁-C₈ perhaloalkoxy, C₁-C₈ alkoxy, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aralkyl, thioalkyl, substituted or unsubstituted amino, alkylsulfonylamino or acyl; or in still a further variation, where R⁴ is independently halo, unsubstituted C₁-C₄ alkyl or C₁-C₄ perhaloalkyl.

In another variation, a compound of the invention is of the formula (I) or (Ia) where X⁷, X⁸, X⁹ and X¹⁰ are taken together to provide an aromatic moiety of the structure:

where each R⁴ is as defined for formula (I) or (Ia); or in a particular variation, where each R⁴ is independently alkyl or halo or in an even more particular variation, where each R⁴ is independently methyl or chloro.

In still a further variation, a compound of the invention is of the formula (I) or (Ia) where X⁷, X⁸, X⁹ and X¹⁰ are taken together provide an aromatic moiety selected from the following structures:

wherein R⁴ is as defined in formula (I); or in a particular variation, where R⁴ is hydroxyl, halo, C₁-C₈ perhaloalkyl, substituted or unsubstituted C₁-C₈ alkyl, substituted or unsubstituted C₂-C₈ alkenyl, substituted or unsubstituted C₂-C₈ alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, C₁-C₈ perhaloalkoxy, C₁-C₈ alkoxy, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aralkyl, thioalkyl, substituted or unsubstituted amino, alkylsulfonylamino or acyl; or in still a further variation, where each R⁴ is independently halo, unsubstituted C₁-C₄ alkyl or C₁-C₄ perhaloalkyl.

In still a further variation, a compound of the invention is of the formula (I) or (Ia) where X⁷, X⁸, X⁹ and X¹⁰ are taken together provide an aromatic moiety of the structure:

wherein R⁴ is as defined in formula (I) or in any particular variation herein, such as when each R⁴ is independently alkyl or halo or in an even more particular variation, where each R⁴ is independently methyl or chloro. In yet another variation, a compound of the invention is of the formula (I) or (Ia) where X⁷, X⁸, X⁹ and X¹⁰ are taken together provide an aromatic moiety of the structure:

In another embodiment, a compound of the invention is of the formula (I), wherein X⁷-X¹⁰ are as defined in formula (I) or as detailed in any variation herein, where R¹ is H, substituted or unsubstituted C₁-C₈ alkyl, acyl, acyloxy, carbonylalkoxy, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted aralkyl. In a further embodiment, a compound of the invention is of the formula (I), wherein X⁷-X¹⁰ are as defined in formula (I) or as detailed in any variation herein, where R¹ is a substituted or unsubstituted C₁-C₈ alkyl, acyl, acyloxy, carbonylalkoxy, substituted or unsubstituted heterocyclyl or substituted or unsubstituted aryl. In a particular variation, a compound of the invention is of the formula (I), wherein X⁷-X¹⁰ are as defined in formula (I) or as detailed in any variation herein, where R¹ is methyl, ethyl, cyclopropyl, propylate, trifluoromethyl, isopropyl, tert-butyl, sec-butyl, 2-methylbutyl, propanal, 1-methyl-2-hydroxyethyl, 2-hydroxyethanal, 2-hydroxyethyl, 2-hydroxypropyl, 2-hydroxy-2-methylpropyl, cyclobutyl, cyclopentyl, cyclohexyl, substituted phenyl, piperidin-4-yl, hydroxycyclopent-3-yl, hydroxycyclopent-2-yl, hydroxycycloprop-2-yl, 1-hydroxy-1-methylcycloprop-2-yl, or 1-hydroxy-1,2,2-trimethyl-cycloprop-3-yl. In another particular variation, a compound of the invention is of the formula (I), wherein X⁷-X¹⁰ are as defined in formula (I) or as detailed in any variation herein, where R¹ is methyl, ethyl, cyclopropyl, propyl, trifluoromethyl, isopropyl, tert-butyl, sec-butyl, 2-methylbutyl, propanoyl, 1-methyl-2-hydroxyethyl, 2-hydroxyethanoyl, 2-hydroxyethyl, 2-hydroxypropyl, 2-hydroxy-2-methylpropyl, cyclobutyl, cyclopentyl, cyclohexyl, substituted phenyl, piperidin-4-yl, hydroxycyclopent-3-yl, hydroxycyclopent-2-yl, hydroxycycloprop-2-yl, 1-hydroxy-1-methylcycloprop-2-yl, or 1-hydroxy-1,2,2-trimethyl-cycloprop-3-yl.

In another variation, the compound of the invention is of the formula (I), where X⁷-X¹⁰ and R¹ are as defined in formula (I) or as detailed in any variation herein, where R^(2a) and R^(2b) are independently H, substituted or unsubstituted C₁-C₈ alkyl, halo, cyano, nitro or R^(2a) and R^(2b) are taken together to form a carbonyl moiety and each R^(3a) and R^(3b) is independently H, substituted or unsubstituted C₁-C₈ alkyl, halo, cyano or nitro. In another variation, the compound of the invention is of the formula (I), where X⁷-X¹⁰ and R¹ are as defined in formula (I) or as detailed in any variation herein, where each R^(2a) and R^(2b) is independently H, unsubstituted C₁-C₈ alkyl, halo or R^(2a) and R^(2b) are taken together to form a carbonyl moiety and each R^(3a) and R^(3b) is independently H, unsubstituted C₁-C₈ alkyl, halo or R^(3a) and R^(3b) are taken together to form a carbonyl moiety. In still a further variation, the compound of the invention is of the formula (I), where X⁷-X¹⁰ and R¹ are as defined in formula (I) or as detailed in any variation herein, where each R^(2a) and R^(2b) is independently H, unsubstituted C₁-C₈ alkyl, halo or R^(2a) and R^(2b) are taken together to form a carbonyl moiety; and each R^(3a) and R^(3b) is independently H, unsubstituted C₁-C₈ alkyl, halo or R^(3a) and R^(3b) are taken together to form a carbonyl moiety. The invention also embraces compounds of the invention according to formula (I), where X⁷-X¹⁰ and R¹ are as defined in formula (I) or as detailed in any variation herein, where each R^(2a) and R^(2b) is independently H, methyl, halo or R^(2a) and R^(2b) are taken together to form a carbonyl moiety and each R^(3a) and R^(3b) is independently H, methyl, halo or R^(3a) and R^(3b) are taken together to form a carbonyl moiety. The invention further embraces compounds of the invention according to formula (I), where X⁷-X¹⁰ and R¹ are as defined in formula (I) or as detailed in any variation herein, where each of R^(2a), R^(2b), R^(3a) and R^(3b) is H. In one variation, a compound of the invention is of the formula (I) where X⁷-X¹⁰ and R¹ are as defined in formula (I) or as detailed in any variation herein, where at least one of R^(2a), R^(2b), R^(3a) and R^(3b) is a substituted or unsubstituted C₁-C₈ alkyl, halo, cyano, nitro or is taken together with a geminal R² or R³ to form a carbonyl moiety. In another variation, a compound of the invention is of the formula (I) where X⁷-X¹⁰ and R¹ are as defined in formula (I) or as detailed in any variation herein, where at least two of R^(2a), R^(2b), R^(3a) and R^(3b) is a substituted or unsubstituted C₁-C₈ alkyl, halo, cyano, nitro or is taken together with a geminal R² or R³ to form a carbonyl moiety. In yet another variation, a compound of the invention is of the formula (I) where X⁷-X¹⁰ and R¹ are as defined in formula (I) or as detailed in any variation herein, where at least one of R^(2a), R^(2b), R^(3a) and R^(3b) is fluoro or methyl or is taken together with a geminal R² or R³ to form a carbonyl moiety. In still another variation, a compound of the invention is of the formula (I) where X⁷-X¹⁰ and R¹ are as defined in formula (I) or as detailed in any variation herein, where either R^(2a) and R^(2b) or R^(3a) and R^(3b) are each methyl or fluoro (e.g., both R^(2a) and R^(2b) are methyl or one is fluoro and one is methyl) or are taken together to form a carbonyl moiety. In one variation, R^(2a) and R^(2b) are taken together to form a carbonyl moiety. In another variation, at least one of R^(2a) and R^(2b) is hydroxyl or alkoxy. In a particular variation, each R^(2a) and R^(2b) is independently H, substituted or unsubstituted C₁-C₈ alkyl, halo, cyano, nitro or R^(2a) and R^(2b) are taken together to form a carbonyl. In another variation, when X¹ is N, each R^(2a) and R^(2b) is independently H, substituted or unsubstituted C₁-C₈ alkyl, halo, cyano, nitro or R^(2a) and R^(2b) are taken together to form a carbonyl.)

The invention also embraces compounds according to formula (I), where X⁷-X¹⁰, R¹, R^(2a), R^(2b), R^(3a) and R^(3b) are as defined in formula (I) or as detailed in any variation herein, where each R^(10a) and R^(10b) is independently H, halo, an unsubstituted C₁-C₈ alkyl, hydroxyl or R^(10a) and R^(10b) are taken together to form a carbonyl. Also embraced are compounds according to formula (I), where X⁷-X¹⁰, R¹, R^(2a), R^(2b), R^(3a) and R^(3b) are as defined in formula (I) or as detailed in any variation herein, where each R^(10a) and R^(10b) is independently H, halo, an unsubstituted C₁-C₄ alkyl, hydroxyl or R^(10a) and R^(10b) are taken together to form a carbonyl. In another variation, a compound of the invention is of the formula (I), where X⁷-X¹⁰, R¹, R^(2a), R^(2b), R^(3a) and R^(3b) are as defined in formula (I) or as detailed in any variation herein, where each R^(10a) and R^(10b) is independently H, bromo, methyl, hydroxyl or R^(10a) and R^(10b) are taken together to form a carbonyl. In yet another variation, a compound of the invention is of the formula (I), where X⁷-X¹⁰, R¹, R^(2a), R^(2b), R^(3a) and R^(3b) are as defined in formula (I) or as detailed in any variation herein, where at least one of R^(10a) and R^(10b) is an unsubstituted C₁-C₈ alkyl, hydroxyl, halo or R^(10a) and R^(10b) are taken together to form a carbonyl. In still a further variation, a compound of the invention is of the formula (I), where X⁷-X¹⁰, R¹, R^(2a), R^(2b), R^(3a) and R^(3b) are as defined in formula (I) or as detailed in any variation herein, where at least one of R^(10a) and R^(10b) is methyl, bromo, hydroxyl or R^(10a) and R^(10b) are taken together to form a carbonyl. In another variation, a compound of the invention is of the formula (I), where X⁷-X¹⁰, R¹, R^(2a), R^(2b), R^(3a) and R^(3b) are as defined in formula (I) or as detailed in any variation herein, where both R^(10a) and R^(10b) are methyl. In another variation, a compound of the invention is of the formula (I), where X⁷-X¹⁰, R¹, R^(2a), R^(2b), R^(3a) and R^(3b) are as defined in formula (I) or as detailed in any variation herein, where R^(10a) and R^(10b) are taken together to form a carbonyl. In another variation, a compound of the invention is of the formula (I), where X⁷-X¹⁰, R¹, R^(2a), R^(2b), R^(3a) and R^(3b) are as defined in formula (I) or as detailed in any variation herein, where R^(10a) is H and R^(10b) is methyl. In another variation, a compound of the invention is of the formula (I), where X⁷-X¹⁰, R¹, R^(2a), R^(2b), R^(3a) and R^(3b) are as defined in formula (I) or as detailed in any variation herein, where R^(10a) is H and R^(10b) is bromo. When the carbon of formula (I) bearing R^(10a) and R^(10b) is optically active, it may be in the S or R configuration and compositions comprising substantially pure R or S compound or mixtures thereof in any amount are embraced by this invention.

In a particular variation, a compound of the invention is of the formula (I) where R^(2a), R^(2b), X¹, R^(10a), R^(10b), R^(3a) and R^(3b) are taken together to form a ring selected from the structures:

where R¹ in the structures above is as defined for formula (I) or any particular variation detailed herein.

In another variation, a compound of the invention is of the formula (I) where R^(2a), R^(2b), X¹, R^(10a), R^(10b), R^(3a) and R^(3b) are taken together to form a ring of the formula:

where R¹ is as defined in formula (I) or any variation detailed herein. In yet another variation, a compound of the invention is of the formula (I) where R^(2a), R^(2b), X¹, R^(10a), R^(10b), R^(3a) and R^(3b) are taken together to form a ring of the formula:

and where X⁷, X⁸, X⁹ and X¹⁰ are taken together provide an aromatic moiety of the structure:

where R¹ is as defined in formula (I) or any variation detailed herein, such as when R¹ is an alkyl group or in a more particular variation when R¹ is methyl, and R⁴ is as defined in formula (I) or in any particular variation herein, such as when each R⁴ is independently alkyl or halo or in an even more particular variation, where each R⁴ is independently methyl or chloro.

Compounds of the formulae (IIa), (IIb), (IIc), (IId), (IIe), (III), (IIg) and (IIh) are also embraced by this invention:

where in each of (IIa), (IIb), (IIc), (IId), (IIe), (IIf), (IIg) and (IIh), R¹, R^(2a), R^(2b), R^(3a), R^(3b), R^(10a), R^(10b), R^(8a)-R^(8f), m, q and Q are as described for formula (I) or any applicable variation thereof. In one variation the invention relates to a compound of the formula (IIa). In another variation the invention relates to a compound of the formula (IIc). Where applicable, in each of (IIa), (IIb), (IIc), (IId), (IIe), (IIf), (IIg) and (IIh), R¹, R^(2a), R^(2b), R^(3a), R^(3b), R^(10a), R^(10b), R^(8a)-R^(8f), m, q and Q may also be as described for any formulae or any applicable variation thereof detailed herein, including but not limited to formulae (A)-(G).

In one variation, the compound is of the formula (IIa), provided that when X¹ is N, the compound is other than any of compounds 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 34x, 35x, 36x, 37x, 44x, 63x, 64x, 65x, 66x, 67x, 69x, 72x, 74x, 76x, 86x and 91x, or a salt thereof. In one variation, the compound is of formula (IIa) wherein X¹ is N, R¹ is methyl and Q is cyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (IIa), including those listed in Table 1, such as 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 34x, 35x, 36x, 37x, 44x, 63x, 64x, 65x, 66x, 67x, 69x, 72x, 74x, 76x, 86x or 91x or a salt thereof.

In one variation, the compound is of the formula (IIc), provided that when X¹ is N, the compound is other than any of compounds 109x and 110x, or a salt thereof. In one variation, the compound is of the formula (IIc) wherein X¹ is N and R₁ is methyl. In another variation, the compound is of the formula (IIc) wherein X¹ is N and Q is carbonylalkoxy, acyloxy, aminoacyl or aminocarbonylalkoxy. In one such variation, the compound is of the formula (IIc) where X¹ is N, R¹ is C₁-C₈ alkyl (e.g., methyl) and Q is carbonylalkoxy, acyloxy, aminoacyl or aminocarbonylalkoxy. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (IIc), including those listed in Table 1, such as 109x or 110x or a salt thereof.

In one variation, the compound is of the formula (IId), provided that when X¹ is N, the compound is other than any of compounds 107x and 108x, or a salt thereof. In another variation, the compound is of the formula (IId) wherein X¹ is N and R¹ is methyl. In a further variation, the compound is of the formula (IId) wherein X¹ is N and Q is carbonylalkoxy, acyloxy, aminoacyl or aminocarbonylalkoxy. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (IId), including those listed in Table 1, such as 107x or 108x or a salt thereof.

Compounds of the formulae (IIIa), (IIIb), (IIIc), (IIId), (IIIe), (IIIf), (IIIg), (IIIh), (IIIi), (IIIj), (IIIk), (IIIl) and (IIIm) are further embraced by this invention:

where in each of (IIIa), (IIIb), (IIIc), (IIId), (IIIe), (IIIf), (IIIg), (IIIh), (IIIi), (IIIj), (IIIk), (IIIl) and (IIIm), R¹, R⁴, R^(2a), R^(2b), R^(3a), R^(3b), R^(10a), R^(10b), R^(8a)R^(8f), m, q and Q are as described for formula (I) or any applicable variation thereof. Where applicable, in each of (IIIa), (IIIb), (IIIc), (IIId), (IIIe), (IIIf), (IIIg), (IIIh), (IIIi), (IIIj), (IIIk), (IIIl) and (IIIm), R¹, R⁴, R^(2a), R^(2b), R^(3a), R^(3b), R^(10a), R^(10b), R^(8a)-R^(8f), m, q and Q may also be as described for any formulae or any applicable variation thereof detailed herein, including but not limited to formulae (A)-(G).

In one variation, the compound is of the formula (IIIa), provided that when X¹ is N, the compound is other than any of compounds 1x, 2x, 3x, 4x, 5x, 6x, 7x, 8x, 9x, 10x, 11x, 12x, 13x, 14x, 15x, 16x, 17x, 18x, 19x, 20x, 21x, 22x, 23x, 24x, 26x, 29x, 30x, 31x, 32x, 33x, 34x, 35x, 36x, 37x, 39x, 40x, 41x, 43x, 44x, 45x, 46x, 47x, 48x, 53x, 54x, 55x, 56x, 57x, 58x, 59x, 60x, 61x, 62x, 63x, 64x, 65x, 66x, 67x, 69x, 70x, 72x, 73x, 74x, 75x, 76x, 78x, 80x, 81x, 82x, 84x, 86x, 87x, 88x, 89x, 90x, 91x, 92x, 96x, 97x, 98x, 99x, 100x, 101x, 102x, 103x, 104x, 105x and 106x, or a salt thereof. In another variation, the compound is of the formula (IIIa), wherein X¹ is N, R⁴ is other than H and Q is acyclic or cyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy. In one such variation, the compound contains one or more of the following structural features: R⁴ is a substituted or unsubstituted C₁-C₈ alkyl (e.g., methyl) or halo (e.g., chloro) and R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) are each H. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (IIIa), including those listed in Table 1, such as 1x, 2x, 3x, 4x, 5x, 6x, 7x, 8x, 9x, 10x, 11x, 12x, 13x, 14x, 15x, 16x, 17x, 18x, 19x, 20x, 21x, 22x, 23x, 24x, 26x, 29x, 30x, 31x, 32x, 33x, 34x, 35x, 36x, 37x, 39x, 40x, 41x, 43x, 44x, 45x, 46x, 47x, 48x, 53x, 54x, 55x, 56x, 57x, 58x, 59x, 60x, 61x, 62x, 63x, 64x, 65x, 66x, 67x, 69x, 70x, 72x, 73x, 74x, 75x, 76x, 78x, 80x, 81x, 82x, 84x, 86x, 87x, 88x, 89x, 90x, 91x, 92x, 96x, 97x, 98x, 99x, 100x, 101x, 102x, 103x, 104x, 105x or 106x or a salt thereof.

In one variation, the compound is of the formula (IIIb), provided that when X¹ is N, the compound is other than any of compounds 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 34x, 35x, 36x, 37x, 44x, 63x, 64x, 65x, 66x, 67x, 69x, 72x, 74x, 76x, 86x and 91x, or a salt thereof. In one variation, the compound is of the formula (IIIb) wherein X¹ is N and R⁴ is chloro. In another variation, the compound is of the formula (IIIb) wherein X¹ is N, R⁴ is chloro and R¹ is methyl. In still another variation, the compound is of the formula (IIIb) wherein X¹ is N, R⁴ is chloro, R¹ is methyl and q is 0. In another variation, the compound is of the formula (IIIb) wherein X¹ is N, R⁴ and R¹ are each methyl and Q is acyclic or cyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy. In yet another variation, the compound is of the formula (IIIb) wherein X¹ is N, R⁴ and R¹ are each methyl and Q is acyclic or cyclic acylamino, aminoacyl or aminocarbonylalkoxy. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (IIIb), including those listed in Table 1, such as 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 34x, 35x, 36x, 37x, 44x, 63x, 64x, 65x, 66x, 67x, 69x, 72x, 74x, 76x, 86x or 91x or a salt thereof.

In one variation, the compound is of the formula (IIIc), provided that when X¹ is N, the compound is other than any of compounds 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 28x, 34x, 35x, 36x, 37x, 44x, 52x, 63x, 64x, 65x, 66x, 67x, 69x, 72x, 74x, 76x, 86x and 91x, or a salt thereof. In another variation, the compound is of the formula (IIIc) wherein X¹ is N, R⁴ is other than H and R¹ is methyl. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (IIIc), including those listed in Table 1, such as 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 28x, 34x, 35x, 36x, 37x, 44x, 52x, 63x, 64x, 65x, 66x, 67x, 69x, 72x, 74x, 76x, 86x or 91x or a salt thereof.

In one variation, the compound is of the formula (IIId), provided that when X¹ is N, the compound is other than any of compounds 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 25x, 27x, 34x, 35x, 36x, 37x, 38x, 42x, 44x, 49x, 50x, 51x, 63x, 64x, 65x, 66x, 67x, 68x, 69x, 71x, 72x, 74x, 76x, 77x, 79x, 83x, 85x, 86x, 91x, 93x, 94x and 95x, or a salt thereof. In anther variation, the compound is of the formula (IIId) wherein X¹ is N, R⁴ is other than hydrogen and Q is acyclic or cyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (IIId), including those listed in Table 1, such as 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 25x, 27x, 34x, 35x, 36x, 37x, 38x, 42x, 44x, 49x, 50x, 51x, 63x, 64x, 65x, 66x, 67x, 68x, 69x, 71x, 72x, 74x, 76x, 77x, 79x, 83x, 85x, 86x, 91x, 93x, 94x or 95x or a salt thereof.

In one variation, the compound is of the formula (IIIe), provided that when X¹ is N, the compound is other than any of compounds 1x, 2x, 3x, 4x, 5x, 6x, 7x, 8x, 9x, 10x, 11x, 12x, 13x, 14x, 15x, 16x, 17x, 18x, 19x, 20x, 21x, 22x, 23x, 24x, 26x, 28x, 29x, 30x, 31x, 32x, 33x, 34x, 35x, 36x, 37x, 39x, 40x, 41x, 43x, 44x, 45x, 46x, 47x, 48x, 52x, 53x, 54x, 55x, 56x, 57x, 58x, 59x, 60x, 61x, 62x, 63x, 64x, 65x, 66x, 67x, 69x, 70x, 72x, 73x, 74x, 75x, 76x, 78x, 80x, 81x, 82x, 84x, 86x, 87x, 88x, 89x, 90x, 91x, 92x, 96x, 97x, 98x, 99x, 100x, 101x, 102x, 103x, 104x, 105x and 106x, or a salt thereof. In another variation, the compound is of the formula (IIIe) wherein X¹ is N, R¹ is methyl and at least one of R⁴ is chloro. In another variation, the compound is of the formula (IIIe) wherein X¹ is N, R¹ is methyl and Q is cyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy. In yet another variation, the compound is of the formula (IIIe) wherein X¹ is N, R¹ is methyl, at least one of R⁴ is methyl and Q is acyclic or cyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy. In yet another variation, the compound is of the formula (IIIe) wherein X¹ is N, R¹ is methyl, at least one of R⁴ is methyl and Q is acyclic or cyclic acylamino, aminocarbonylalkoxy, or acylamino. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (IIe), including those listed in Table 1, such as 1x, 2x, 3x, 4x, 5x, 6x, 7x, 8x, 9x, 10x, 11x, 12x, 13x, 14x, 15x, 16x, 17x, 18x, 19x, 20x, 21x, 22x, 23x, 24x, 26x, 28x, 29x, 30x, 31x, 32x, 33x, 34x, 35x, 36x, 37x, 39x, 40x, 41x, 43x, 44x, 45x, 46x, 47x, 48x, 52x, 53x, 54x, 55x, 56x, 57x, 58x, 59x, 60x, 61x, 62x, 63x, 64x, 65x, 66x, 67x, 69x, 70x, 72x, 73x, 74x, 75x, 76x, 78x, 80x, 81x, 82x, 84x, 86x, 87x, 88x, 89x, 90x, 91x, 92x, 96x, 97x, 98x, 99x, 100x, 101x, 102x, 103x, 104x, 105x or 106x or a salt thereof.

In one variation, the compound is of the formula (IIIf), provided that when X¹ is N, the compound is other than any of compounds 107x and 108x, or a salt thereof. In yet another variation, the compound is of the formula (IIIf) wherein X¹ is N and R¹ is methyl. In yet another variation, the compound is of the formula (IIIf) wherein X¹ is N and at least one of m and q is 1. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (IIIf), including those listed in Table 1, such as 107x or 108x or a salt thereof.

In one variation, the compound is of the formula (IIIk), provided that when X¹ is N, the compound is other than any of compounds 1x, 2x, 3x, 4x, 5x, 6x, 7x, 8x, 9x, 10x, 11x, 12x, 13x, 14x, 15x, 16x, 17x, 18x, 19x, 20x, 21x, 22x, 23x, 24x, 25x, 26x, 27x, 29x, 30x, 31x, 32x, 33x, 34x, 35x, 36x, 37x, 38x, 39x, 40x, 41x, 42x, 43x, 44x, 45x, 46x, 47x, 48x, 49x, 50x, 51x, 53x, 54x, 55x, 56x, 57x, 58x, 59x, 60x, 61x, 62x, 63x, 64x, 65x, 66x, 67x, 68x, 69x, 70x, 71x, 72x, 73x, 74x, 75x, 76x, 77x, 78x, 79x, 80x, 81x, 82x, 83x, 84x, 85x, 86x, 87x, 88x, 89x, 90x, 91x, 92x, 93x, 94x, 95x, 96x, 97x, 98x, 99x, 100x, 101x, 102x, 103x, 104x, 105x and 106x, or a salt thereof. In another variation, the compound is of the formula (IIIk) wherein X¹ is N, R¹ is methyl, at least one R⁴ is methyl or chloro and Q is acyclic or cyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy. In yet another variation, the compound is of the formula (IIIk) wherein X¹ is N, R¹ is methyl, at least one R⁴ is methyl or chloro and Q is acyclic or cyclic acylamino, aminoacyl or aminocarbonylalkoxy. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (IIIk), including those listed in Table 1, such as 1x, 2x, 3x, 4x, 5x, 6x, 7x, 8x, 9x, 10x, 11x, 12x, 13x, 14x, 15x, 16x, 17x, 18x, 19x, 20x, 21x, 22x, 23x, 24x, 25x, 26x, 27x, 29x, 30x, 31x, 32x, 33x, 34x, 35x, 36x, 37x, 38x, 39x, 40x, 41x, 42x, 43x, 44x, 45x, 46x, 47x, 48x, 49x, 50x, 51x, 53x, 54x, 55x, 56x, 57x, 58x, 59x, 60x, 61x, 62x, 63x, 64x, 65x, 66x, 67x, 68x, 69x, 70x, 71x, 72x, 73x, 74x, 75x, 76x, 77x, 78x, 79x, 80x, 81x, 82x, 83x, 84x, 85x, 86x, 87x, 88x, 89x, 90x, 91x, 92x, 93x, 94x, 95x, 96x, 97x, 98x, 99x, 100x, 101x, 102x, 103x, 104x, 105x or 106x or a salt thereof.

In one variation, the compound is of the formula (IIIl), provided that when X¹ is N, the compound is other than any of compounds 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 28x, 34x, 35x, 36x, 37x, 44x, 52x, 63x, 64x, 65x, 66x, 67x, 69x, 72x, 74x, 76x, 86x and 91x, or a salt thereof. In another variation, the compound is of the formula (IIIl) wherein X¹ is N, R¹ is methyl and at least one of R⁴ is other than H. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (IIIl), including those listed in Table 1, such as 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 28x, 34x, 35x, 36x, 37x, 44x, 52x, 63x, 64x, 65x, 66x, 67x, 69x, 72x, 74x, 76x, 86x or 91x or a salt thereof.

In one variation, the compound is of the formula (IIIm), provided that when X¹ is N, the compound is other than any of compounds 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 25x, 27x, 34x, 35x, 36x, 37x, 38x, 42x, 44x, 49x, 50x, 51x, 63x, 64x, 65x, 66x, 67x, 68x, 69x, 71x, 72x, 74x, 76x, 77x, 79x, 83x, 85x, 86x, 91x, 93x, 94x and 95x, or a salt thereof. In another variation, the compound is of the formula (IIIm) wherein X¹ is N and each R⁴ is other than H. In another variation, the compound is of the formula (IIIm) wherein X¹ is N, R¹ is methyl and Q is cyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (IIIm), including those listed in Table 1, such as 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 25x, 27x, 34x, 35x, 36x, 37x, 38x, 42x, 44x, 49x, 50x, 51x, 63x, 64x, 65x, 66x, 67x, 68x, 69x, 71x, 72x, 74x, 76x, 77x, 79x, 83x, 85x, 86x, 91x, 93x, 94x or 95x or a salt thereof.

Compounds of the formulae (IVa), (IVb), (IVc), (IVd), (IVe), (IVf), (IVg), (IVh), (IVi), (IVj) and (IVk) are further embraced by this invention:

where in each of (IVa), (IVb), (IVc), (IVd), (IVe), (IVf), (IVg), (IVh), (IVi), (IVj) and (IVk), R¹, X⁷, X⁸, X⁹, X¹⁰, R^(8a)-R^(8f), m, q and Q are as described for formula (I) or any applicable variation thereof. Where applicable, in each of (IVa), (IVb), (IVc), (IVd), (IVe), (IVf), (IVg), (IVh), (IVi), (IVj) and (IVk), R¹, X⁷, X⁸, X⁹, X¹⁰, R^(8a)-R^(8f), m, q and Q may also be as described for any formulae or any applicable variation thereof detailed herein, including but not limited to formulae (A)-(G).

In one variation, the compound is of the formula (IVa), provided that the compound is other than any of compounds 1x, 2x, 3x, 4x, 5x, 6x, 7x, 8x, 9x, 10x, 11x, 12x, 13x, 14x, 15x, 16x, 17x, 18x, 19x, 20x, 21x, 22x, 23x, 24x, 25x, 26x, 27x, 28x, 29x, 30x, 31x, 32x, 33x, 34x, 35x, 36x, 37x, 38x, 39x, 40x, 41x, 42x, 43x, 44x, 45x, 46x, 47x, 48x, 49x, 50x, 51x, 52x, 53x, 54x, 55x, 56x, 57x, 58x, 59x, 60x, 61x, 62x, 63x, 64x, 68x, 69x, 70x, 71x, 72x, 73x, 74x, 75x, 76x, 77x, 78x, 79x, 80x, 81x, 82x, 83x, 84x, 85x, 86x, 87x, 88x, 89x, 90x, 91x, 92x, 93x, 94x, 95x, 97x, 98x, 99x, 100x, 101x, 102x, 103x, 104x, 105x, 106x, 107x, 108x, 109x and 110x, or a salt thereof. In one variation, the compound is of the formula (IVa) wherein m and q are each 1. In one such variation, m and q are each 1 and R¹ is methyl. In another such variation, m and q are each 1 and R¹ is methyl and X⁹ is N or CR⁴ where R⁴ is C₁-C₈alkyl (e.g., methyl) or halo (e.g., chloro). In another variation, the compound is of the formula (IVa) wherein R¹ is methyl and Q is cyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy. In another variation, the compound is of the formula (IVa) wherein R¹ is methyl and at least one of X⁷-X¹⁰ is CR₄ where R₄ is chloro. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (IVa), including those listed in Table 1, such as 1x, 2x, 3x, 4x, 5x, 6x, 7x, 8x, 9x, 10x, 11x, 12x, 13x, 14x, 15x, 16x, 17x, 18x, 19x, 20x, 21x, 22x, 23x, 24x, 25x, 26x, 27x, 28x, 29x, 30x, 31x, 32x, 33x, 34x, 35x, 36x, 37x, 38x, 39x, 40x, 41x, 42x, 43x, 44x, 45x, 46x, 47x, 48x, 49x, 50x, 51x, 52x, 53x, 54x, 55x, 56x, 57x, 58x, 59x, 60x, 61x, 62x, 63x, 64x, 68x, 69x, 70x, 71x, 72x, 73x, 74x, 75x, 76x, 77x, 78x, 79x, 80x, 81x, 82x, 83x, 84x, 85x, 86x, 87x, 88x, 89x, 90x, 91x, 92x, 93x, 94x, 95x, 97x, 98x, 99x, 100x, 101x, 102x, 103x, 104x, 105x, 106x, 107x, 108x, 109x or 110x or a salt thereof.

The invention also embraces compounds of the formulae (Va)-(Vzf):

where in each of (Va)-(Vzf), R′, R⁴, R^(8a)—R^(8f), m, q and Q are as described for formula (I) or any applicable variation thereof. In one variation the invention relates to a compound of the formula (Vc) or (Vf). Where applicable, in each of (Va)-(Vzf), R¹, R⁴, R^(8a)-R^(8f), m, q and Q may also be as described for any formulae or any applicable variation thereof detailed herein, including but not limited to formulae (A)-(G).

In one variation, the compound is of the formula (Va), provided that the compound is other than any of compounds 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 34x, 35x, 36x, 37x, 44x, 63x, 64x, 69x, 72x, 74x, 76x, 86x and 91x, or a salt thereof. In one variation, the compound is of the formula (Va) wherein at least one of (i)-(iv) apply: (i) at least one of m and q is 1 and Q is cyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy; (ii) Q is aminoacyl or aminocarvonylalkoxy; (iii) R¹ is methyl and Q is cyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy; (iv) both m and q are 1. In one variation, at least two of (i)-(iv) apply. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (Va), including those listed in Table 1, such as 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 34x, 35x, 36x, 37x, 44x, 63x, 64x, 69x, 72x, 74x, 76x, 86x or 91x or a salt thereof.

In one variation, the compound is of the formula (Vc), provided that the compound is other than any of compounds 109x and 110x, or a salt thereof. In another variation, the compound is of the formula (Vc) wherein at least one of (i)-(iii) apply: (i) R¹ is methyl; (ii) at least one of m and q is 1; (iii) Q is carbonylalkoxy, acyloxy, aminoacyl or aminocarbonylalkoxy. In one such variation, at least two of (i)-(iii) apply. In yet another variation, the compound is of the formula (Vc) wherein Q is aminoacyl or carbonyl alkoxy. In still another variation, the compound is of the formula (Vc) wherein Q is aminoacyl or carbonyl alkoxy and R¹ is methyl. In one variation, the compound is of the formula (Vc) where R¹ is other than isopropyl. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (Vc), including those listed in Table 1, such as 109x or 110x or a salt thereof.

In one variation, the compound is of the formula (Vd), provided that the compound is other than any of compounds 107x and 108x, or a salt thereof. In anther variation, the compound is of the formula (Vd) wherein Q is carbonylalkoxy, acyloxy, aminoacyl or aminocarbonylalkoxy. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (Vd), including those listed in Table 1, such as 107x or 108x or a salt thereof.

In one variation, the compound is of the formula (Ve), provided that the compound is other than any of compounds 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 34x, 35x, 36x, 37x, 44x, 63x, 64x, 69x, 72x, 74x, 76x, 86x and 91x, or a salt thereof. In one variation, the compound is of the formula (Ve) wherein Q is aminoacyl or aminocarbonylalkoxy. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (Ve), including those listed in Table 1, such as 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 34x, 35x, 36x, 37x, 44x, 63x, 64x, 69x, 72x, 74x, 76x, 86x or 91x or a salt thereof.

In one variation, the compound is of the formula (Vf), provided that the compound is other than any of compounds 1x, 2x, 3x, 4x, 5x, 6x, 7x, 8x, 9x, 10x, 11x, 12x, 13x, 14x, 15x, 16x, 17x, 18x, 19x, 20x, 21x, 22x, 23x, 24x, 26x, 29x, 30x, 31x, 32x, 33x, 34x, 35x, 36x, 37x, 39x, 40x, 41x, 43x, 44x, 45x, 46x, 47x, 48x, 53x, 54x, 55x, 56x, 57x, 58x, 59x, 60x, 61x, 62x, 63x, 64x, 69x, 70x, 72x, 73x, 74x, 75x, 76x, 78x, 80x, 81x, 82x, 84x, 86x, 87x, 88x, 89x, 90x, 91x, 92x, 97x, 98x, 99x, 100x, 101x, 102x, 103x, 104x, 105x and 106x, or a salt thereof. In one variation, the compound is of the formula (Vf) wherein R¹ is methyl and Q is cyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy. In another variation, the compound is of the formula (Vf) wherein m and q are each 1. In another variation, the compound is of the formula (Vf) wherein R¹ is methyl and R⁴ is chloro. In yet another variation, the compound is of the formula (Vf) wherein R¹ is methyl, R⁴ is methyl and Q is acyclic or cyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy. In another variation, the compound is of the formula (Vf) wherein R¹ is methyl, R⁴ is methyl and Q is acyclic or cyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy. In one variation, the compound is of the formula (Vf) where R¹ is methyl, R⁴ is other than H and Q is other than —C(O)O-ethyl. In another variation, the compound is of the formula (Vf) where R¹ and R⁴ are methyl and Q is other than —C(O)O-ethyl. In yet another variation, the compound is of the formula (Vf) where R¹ and R⁴ are methyl and Q is acyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (Vf), including those listed in Table 1, such as lx, 2x, 3x, 4x, 5x, 6x, 7x, 8x, 9x, 10x, 11x, 12x, 13x, 14x, 15x, 16x, 17x, 18x, 19x, 20x, 21x, 22x, 23x, 24x, 26x, 29x, 30x, 31x, 32x, 33x, 34x, 35x, 36x, 37x, 39x, 40x, 41x, 43x, 44x, 45x, 46x, 47x, 48x, 53x, 54x, 55x, 56x, 57x, 58x, 59x, 60x, 61x, 62x, 63x, 64x, 69x, 70x, 72x, 73x, 74x, 75x, 76x, 78x, 80x, 81x, 82x, 84x, 86x, 87x, 88x, 89x, 90x, 91x, 92x, 97x, 98x, 99x, 100x, 101x, 102x, 103x, 104x, 105x or 106x or a salt thereof.

In one variation, the compound is of the formula (Vg), provided that the compound is other than any of compounds 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 28x, 34x, 35x, 36x, 37x, 44x, 52x, 63x, 64x, 69x, 72x, 74x, 76x, 86x and 91x, or a salt thereof. In one variation, the compound is of the formula (Vg) wherein at least one of (i)-(iii) applies: (1) both of m and q are 1; (2) when one of m and q is 1 and the other is 0, then R⁴ is other than H; (3) Q is aminoacyl or aminocarbonylalkoxy. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (Vg), including those listed in Table 1, such as 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 28x, 34x, 35x, 36x, 37x, 44x, 52x, 63x, 64x, 69x, 72x, 74x, 76x, 86x or 91x or a salt thereof.

In one variation, the compound is of the formula (Vh), provided that the compound is other than any of compounds 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 25x, 27x, 34x, 35x, 36x, 37x, 38x, 42x, 44x, 49x, 50x, 51x, 63x, 64x, 68x, 69x, 71x, 72x, 74x, 76x, 77x, 79x, 83x, 85x, 86x, 91x, 93x, 94x and 95x, or a salt thereof. In one variation, the compound is of the formula (Vh) wherein at least one of (i)-(iii) applies: (1) both of m and q are 1; (2) when one of m and q is 1 and the other is 0, then Q cyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy; (3) Q is aminoacyl or aminocarbonylalkoxy. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (Vh), including those listed in Table 1, such as 11x, 14x, 15x, 16x, 17x, 18x, 19x, 21x, 22x, 23x, 24x, 25x, 27x, 34x, 35x, 36x, 37x, 38x, 42x, 44x, 49x, 50x, 51x, 63x, 64x, 68x, 69x, 71x, 72x, 74x, 76x, 77x, 79x, 83x, 85x, 86x, 91x, 93x, 94x and 95x or a salt thereof.

In one variation, the compound is of the formula (Vn), provided that the compound is other than any of compounds 1x, 2x, 3x, 4x, 5x, 6x, 7x, 8x, 9x, 10x, 11x, 12x, 13x, 14x, 15x, 16x, 17x, 18x, 19x, 20x, 21x, 22x, 23x, 24x, 26x, 28x, 29x, 30x, 31x, 32x, 33x, 34x, 35x, 36x, 37x, 39x, 40x, 41x, 43x, 44x, 45x, 46x, 47x, 48x, 52x, 53x, 54x, 55x, 56x, 57x, 58x, 59x, 60x, 61x, 62x, 63x, 64x, 69x, 70x, 72x, 73x, 74x, 75x, 76x, 78x, 80x, 81x, 82x, 84x, 86x, 87x, 88x, 89x, 90x, 91x, 92x, 97x, 98x, 99x, 100x, 101x, 102x, 103x, 104x, 105x and 106x, or a salt thereof. In one variation, the compound is of the formula (Vn) wherein R¹ is methyl and at least one of (i)-(iii) applies: (i) at least one of R⁴ is chloro; (ii) m and q are each 1; and (iii) Q is cyclic acylamino, acyloxy, aminoacyl or aminocarbonylalkoxy. In one such variation, at least two of (i)-(iii) apply. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (Vn), including those listed in Table 1, such as 1x, 2x, 3x, 4x, 5x, 6x, 7x, 8x, 9x, 10x, 11x, 12x, 13x, 14x, 15x, 16x, 17x, 18x, 19x, 20x, 21x, 22x, 23x, 24x, 26x, 28x, 29x, 30x, 31x, 32x, 33x, 34x, 35x, 36x, 37x, 39x, 40x, 41x, 43x, 44x, 45x, 46x, 47x, 48x, 52x, 53x, 54x, 55x, 56x, 57x, 58x, 59x, 60x, 61x, 62x, 63x, 64x, 69x, 70x, 72x, 73x, 74x, 75x, 76x, 78x, 80x, 81x, 82x, 84x, 86x, 87x, 88x, 89x, 90x, 91x, 92x, 97x, 98x, 99x, 100x, 101x, 102x, 103x, 104x, 105x or 106x or a salt thereof.

In one variation, the compound is of the formula (Vo), provided that the compound is other than any of compounds 107x and 108x, or a salt thereof. In one variation, the compound is of the formula (Vo) wherein R¹ is methyl. In another variation, the compounds of the invention, and methods of using the compounds detailed herein, encompass any of the compounds of formula (Vo), including those listed in Table 1, such as 107x or 108x or a salt thereof.

In one variation, a compound of the invention is of the formula (I) or (Ia) or any variation of the foregoing detailed herein, or is of any one of the formulae (IIa)-(IIh), (IIIa)-(IIIm), (IVa)-(IVk) or (Va)-(Vzf), where each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is independently H, hydroxyl, unsubstituted C₁-C₄ alkyl or is taken together with the carbon to which it is attached and a geminal R^(8(e-f)) to form a cycloalkyl moiety. Where applicable, such variations apply equally to any formulae detailed herein, such as formula (A)-(G). In another variation, a compound of the invention is of the formula (I) or (Ia) or any variation of the foregoing detailed herein, or is of any one of the formulae (IIa)-(IIh), (IIIa)-(IIIm), (IVa)-(IVk) or (Va)-(Vzf), where each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is independently H, hydroxyl, methyl or is taken together with the carbon to which it is attached and a geminal R^(8(a-f)) to form a cyclopropyl moiety. Where applicable, such variations apply equally to any formulae detailed herein, such as formula (A)-(G). In yet another variation, a compound of the invention is of the formula (I) or (Ia) or any variation of the foregoing detailed herein, or is any one of the formulae (IIa)-(IIh), (IIIa)-(IIIm), (IVa)-(IVk) or (Va)-(Vzf), where wherein q is 0 and m is 1. Where applicable, such variations apply equally to any formulae detailed herein, such as formula (A)-(G). The invention also embraces a compound of the invention according to formula (I) or (Ia) or any variation of the foregoing detailed herein, or a compound according to any one of the formulae (IIa)-(IIh), (IIIa)-(IIIm), (IVa)-(IVk) or (Va)-(Vzf), where q and m are both 0. Where applicable, such variations apply equally to any formulae detailed herein, such as formula (A)-(G). The invention further embraces a compound according to formula (I) or (Ia) or any variation of the foregoing detailed herein, or a compound according to any one of the formulae (IIa)-(IIh), (IIIa)-(IIIm), (IVa)-(IVk) or (Va)-(Vzf), where q, m, R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) are taken together to form a moiety selected from the group consisting of: —CH₂—, —CH₂CH₂—, —CH₂CH₂CH₂—, —CH₂—C(H)(OH)—, —C(H)(OH)—CH₂—, —CH₂—C(OH)(CH₃)—, —C(OH)(CH₃)—CH₂—, —CH₂—C(H)(CH₃)—, —C(H)(CH₃)—CH₂—, —CH₂—C(CH₃)(CH₃)—, —C(CH₂CH₂)—CH₂— and —CH₂—C(CH₂CH₂)—. Where applicable, such variations apply equally to any formulae detailed herein, such as formula (A)-(G).

In another variation, a compound of the invention is of the formula (I) or (Ia) or any variation of the foregoing detailed herein, or a compound according to any one of the formulae (IIIa)-(IIIm), (IVa)-(IVk) or (Va)-(Vzf), where each R⁴ is independently H, halo, substituted or unsubstituted C₁-C₈ alkyl, C₁-C₈ perhaloalkyl, substituted or unsubstituted heterocyclyl or a substituted or unsubstituted aryl. In yet another variation, a compound of the invention is of the formula (I) or (Ia) or any variation of the foregoing detailed herein, or a compound according to any one of the formulae (IIIa)-(IIIm), (IVa)-(IVk) or (Va)-(Vzf), where each R⁴ is independently H or a substituted or unsubstituted C₁-C₈ alkyl. In still another variation, a compound of the invention is of the formula (I) or (Ia) or any variation of the foregoing detailed herein, or a compound according to any one of the formulae (IIIa)-(IIIm), (IVa)-(IVk) or (Va)-(Vzf), where each R⁴ is H. The invention also embraces compounds of the formula (I) or (Ia) or any variation of the foregoing detailed herein, or a compound according to any one of the formulae (IIIa)-(IIIm), (IVa)-(IVk) or (Va)-(Vzf), where each R⁴ is independently H, halo, unsubstituted C₁-C₄ alkyl, C₁-C₄ perhaloalkyl or a substituted or unsubstituted aryl. The invention further embraces compounds of the formula (I) or (Ia) or any variation of the foregoing detailed herein, or a compound according to any one of the formulae (IIIa)-(IIIm), (IVa)-(IVk) or (Va)-(Vzf) where each R⁴ is independently H, halo, methyl, perfluoromethyl or cyclopropyl.

The invention also embraces compounds of the formula (I), (E) or (Ia) or any variation of the foregoing detailed herein, or a compound according to any one of the formulae (IIa)-(IIh), (IIIa)-(IIIm), (IVa)-(IVk) or (Va)-(Vzf) where Q is an aminoacyl moiety. In one variation, Q is an aminoacyl group where at least one of R_(a) and R_(b) is H, such as when Q is of the formula —NHC(O)R_(b). In one variation, Q is an aminoacyl moiety selected from the group consisting of: —NHC(O)-heterocyclyl, —NHC(O)-substituted heterocyclyl, —NHC(O)-alkyl, —NHC(O)-cycloalkyl, —NHC(O)-alkaryl and —NHC(O)-substituted aryl. In another variation, Q is an aminoacyl moiety selected from the group consisting of: —NHC(O)—C₅-C₇heterocyclyl, —NHC(O)—C₁-C₆alkyl, —NHC(O)—C₃-C₇cycloalkyl, —NHC(O)—C₁-C₃alkaryl and —NHC(O)-substituted phenyl. In a particular variation, Q is a moiety of the formula:

In one variation, a compound of the invention is of the formula (I), (E) or (Ia) or any variation of the foregoing detailed herein, or a compound according to any one of the formulae (IIa)-(IIh), (IIIa)-(IIIm), (IVa)-(IVk) or (Va)-(Vzf) where Q is acyloxy.

In one variation, a compound of the invention is of the formula (I), (E) or (Ia) or any variation of the foregoing detailed herein, or a compound according to any one of the formulae (IIa)-(IIh), (IIIa)-(IIIm), (IVa)-(IVk) or (Va)-(Vzf) where Q is a carbonylalkoxy moiety. In one variation, Q is a carbonylalkoxy moiety of the formula —C(O)—O—R where R is H, alkyl, substituted alkyl or alkaryl. In one variation, Q is carbonylalkoxy moiety of the formula —C(O)—O—C₁-C₆alkyl. In a particular variation, Q is a carbonylalkoxy moiety of the formula —C(O)—O—C₂H₅. In one variation, Q is a carbonylalkoxy moiety selected from the group consisting of: —C(O)—O—C₁-C₁₀alkyl, —C(O)—O—C₁-C₃alkaryl, —C(O)—O—C₁-C₃substituted alkyl and —C(O)—OH. In another variation, Q is —C(O)—O—C₁-C₆alkyl. In a particular variation, Q is a moiety of the formula:

In another particular variation, Q is a moiety of the formula:

In another variation, a compound of the invention is of the formula (I), (E) or (Ia) or any variation of the foregoing detailed herein, or a compound according to any one of the formulae (IIa)-(IIh), (IIIa)-(IIIm), (IVa)-(IVk) or (Va)-(Vzf) where Q is an aminocarbonylalkoxy moiety. In one variation, Q is an aminocarbonylalkoxy moiety of the formula —NHC(O)—O—R_(b). In another variation, Q is an aminocarbonylalkoxy moiety of the formula —NHC(O)—O—R_(b) where R_(b) is a substituted alkyl group. In a particular variation, Q is a moiety of the formula —NH—C(O)—O—CH₂—C(Cl)₃.

The invention also embraces compounds of the formula (I), (E) or (Ia) or any variation of the foregoing detailed herein, or a compound according to any one of the formulae (IIa)-(IIh), (IIIa)-(IIIm), (IVa)-(IVk) or (Va)-(Vzf) where Q is an acylamino moiety. In one variation, Q is an acylamino group where at least one of R_(a) and R_(b) is H, such as when Q is of the formula —C(O)N(H)(R_(b)). In another variation, Q is an acylamino group where both R_(a) and R_(b) are alkyl. In one variation, Q is an acylamino moiety selected from the group consisting of: —C(O)—N(H)(alkyl), —C(O)—N(alkyl)₂, —C(O)—N(H)(alkaryl) and —C(O)—N(H)(aryl). In another variation, Q is an acylamino moiety selected from the group consisting of: —C(O)—N(H)₂, —C(O)—N(H)(C₁-C₈alkyl), —C(O)—N(C₁-C₆alkyl)₂ and —C(O)—N(H)(C₁-C₃alkaryl). In a particular variation, Q is a moiety of the formula:

In yet a further variation, a compound of the invention is of the formula (I) where R¹ is a substituted or unsubstituted C₁-C₈ alkyl, acyl, acyloxy, carbonylalkoxy, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aryl; each R^(2a) and R^(2b) is independently H, unsubstituted C₁-C₈ alkyl or halo; each R^(3a) and R^(3b) is independently H or halo; each X⁷, X⁸, X⁹ and X¹⁰ is CR⁴, where R⁴ is as defined in formula (I) or in a particular variation, R⁴ is H, halo, pyridyl, methyl or trifluoromethyl; R^(10a) and R^(10b) are both H. In one variation, a compound of the variation detailed herein is provided wherein R¹ is propylate, methyl, ethyl, cyclopropyl, trifluoromethyl, isopropyl, tert-butyl, sec-butyl, 2-methylbutyl, propanal, 1-methyl-2-hydroxyethyl, 2-hydroxyethanal, 2-hydroxyethyl, 2-hydroxypropyl, 2-hydroxy-2-methylpropyl, cyclobutyl, cyclopentyl, cyclohexyl, substituted phenyl, piperidin-4-yl, hydroxycyclopent-3-yl, hydroxycyclopent-2-yl, hydroxycycloprop-2-yl, 1-hydroxy-1-methylcycloprop-2-yl, or 1-hydroxy-1,2,2-trimethyl-cycloprop-3-yl. In another variation, a compound of the variation detailed herein is provided wherein R¹ is propyl, methyl, ethyl, cyclopropyl, trifluoromethyl, isopropyl, tert-butyl, sec-butyl, 2-methylbutyl, propanoyl, 1-methyl-2-hydroxyethyl, 2-hydroxyethanoyl, 2-hydroxyethyl, 2-hydroxypropyl, 2-hydroxy-2-methylpropyl, cyclobutyl, cyclopentyl, cyclohexyl, substituted phenyl, piperidin-4-yl, hydroxycyclopent-3-yl, hydroxycyclopent-2-yl, hydroxycycloprop-2-yl, 1-hydroxy-1-methylcycloprop-2-yl, or 1-hydroxy-1,2,2-trimethyl-cycloprop-3-yl.

In still a further variation, a compound of the invention is of the formula (I) where R¹ is a substituted or unsubstituted C₁-C₈ alkyl; each R^(2a), R^(2b), R^(3a) and R^(3b) is independently H or halo; X¹ is N; each R⁴ is independently H, halo, C₁-C₈ perhaloalkyl, substituted or a unsubstituted C₁-C₈ alkyl; R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H. The invention also embraces a compound of the formula (I) where R¹ is a methyl; at least one of X⁷, X⁸, X⁹ and X¹⁰ is CR⁴, and each R⁴ is independently H, halo, methyl or trifluoromethyl.

In a particular variation, the compound is of the formula (I) where R¹ is a substituted or unsubstituted C₁-C₈ alkyl; each R^(2a) and R^(2b) is independently H, a substituted or unsubstituted C₁-C₈ alkyl or R^(2a) and R^(2b) are taken together to form a carbonyl moiety; R^(3a) and R^(3b) are both H; X¹ is N, each R⁴ is independently H, halo or substituted or unsubstituted C₁-C₈ alkyl; each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is H; each R^(10a) and R^(10b) is independently H, halo, a substituted or unsubstituted C₁-C₈ alkyl, hydroxyl, alkoxyl or R^(10a) and R^(10b) are taken together to form a carbonyl, provided that at least one of R^(10a) and R^(10b) is other than H. In yet another aspect of this variation, X⁷, X⁸, X⁹ and X¹⁰ are CR⁴ and each R⁴ is independently H, halo or methyl.

Examples of compounds according to the invention are depicted in Table 2. The compounds depicted may be present as salts even if salts are not depicted and it is understood that the invention embraces all salts and solvates of the compounds depicted here, as well as the non-salt and non-solvate form of the compound, as is well understood by the skilled artisan.

TABLE 2 Representative Compounds According to the Invention. Compound No. Structure CD#  1

CD2   2

CD3   3

CD4   4

CD5   5

CD6   6

CD7   7

CD8   8

CD9   9

CD10 10

CD11 11

CD12 12

CD13 13

CD14 14

CD15 15

CD16 16

CD17 17

CD18 18

CD19 19

CD20 20

CD21 21

CD22 22

CD23 23

CD24 24

CD25 25

CD26 26

CD27 27

CD28 28

CD29 29

CD30 30

CD31 31

CD32 32

CD33 33

CD34 34

CD35 35

CD36 36

CD37 37

CD38 38

CD39 39

CD40 40

CD41 41

CD42 42

CD43 43

CD44 44

CD45 45

CD48 46

CD49 47

CD50 48

CD51 49

CD52 50

CD53 51

CD54 52

CD56 53

CD60 54

CD64 55

CD65 56

CD66 57

CD67 58

CD69 59

CD74 60

CD75 61

CD76 62

CD77 63

CD78 64

CD79 65

CD80 66

CD81 67

CD82 68

CD83 69

CD84 70

CD72 71

72

73

Also embraced by the invention is a compound of the formula (G):

or a salt thereof,

where:

R^(1a) is alkyl;

R^(4a) is selected from alkyl, aryl, and substituted aryl;

R⁵ is alkyl; and

R^(8g) is selected from alkyl, substituted alkyl and aralkyl.

In one variation of the formula (G), R^(8g) is alkyl, e.g. methyl or isopropyl. In another variation of the formula (G), R^(8g) is substituted alkyl substituted with one or more alkyl or alkoxy groups. In yet another variation, of the formula (G), R^(8g) is substituted alkyl substituted with an alkoxy group, e.g. methoxymethyl. In yet another variation, R^(8g) is substituted aralkyl where the aryl moiety of the aralkyl is at least 3 carbon atoms removed from the carbon to which R^(8g) is attached, e.g. 3-phenylpropyl.

In some embodiments, R^(8g) is selected from alkyl, substituted alkyl, and alkyl-phenyl. In some embodiments, R^(8g) is selected from C₁-C₄ alkyl, substituted C₁-C₄ alkyl, and C₁-C₄ alkyl-phenyl. In some embodiments, R^(8g) is selected from methyl, isopropyl, methoxymethyl, and benzyl.

In some embodiments, R^(4a) is selected from alkyl, phenyl, and substituted phenyl. In some embodiments, R^(4a) is selected from C₁-C₄ alkyl, phenyl, and phenyl substituted with a C₁-C₄ alkoxy or C₁-C₄ alkyl moiety. In some embodiments, R^(4a) is selected from methyl, phenyl, 4-methoxyphenyl, and 4-methylphenyl.

In some embodiments, R^(1a) is C₁-C₄ alkyl. In some embodiments, R^(1a) is methyl.

In some embodiments, R⁵ is C₁-C₄ alkyl. In some embodiments, R⁵ is ethyl.

In one variation, R^(1a) is methyl, R⁵ is ethyl and R^(8g) and R^(4a) are as defined by any variation herein.

In some embodiments, R^(4a) is methyl, R^(1a) is methyl, R⁵ is ethyl, and R^(8g) is selected from alkyl, substituted alkyl, and C₁-C₄ aralkyl, where the aralkyl group is attached to the parent residue via the alkyl moiety.

In some embodiments, R^(4a) is methyl, R^(1a) is methyl, R⁵ is ethyl, and R^(8g) is selected from C₁-C₄ alkyl, substituted C₁-C₄ alkyl, and C₁-C₄ alkyl-phenyl.

In some embodiments, R^(4a) is methyl, R^(1a) is methyl, R⁵ is ethyl, and R^(8g) is selected from methyl, isopropyl, methoxymethyl, and benzyl.

In some embodiments, R^(8g) is methyl, R^(1a) is methyl, R⁵ is ethyl, and R^(4a) is selected from alkyl, phenyl, and substituted phenyl.

In some embodiments, R^(8g) is methyl, R^(1a) is methyl, R⁵ is ethyl, and R^(4a) is selected from C₁-C₄ alkyl, phenyl, and phenyl substituted with a C₁-C₄ alkoxy or C₁-C₄ alkyl moiety.

In some embodiments, R^(8g) is methyl, R^(1a) is methyl, R⁵ is ethyl, and R^(4a) is selected from methyl, phenyl, 4-methoxyphenyl, and 4-methylphenyl.

In some embodiments, the compound is selected from ethyl 2-(2,8-dimethyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)propanoate; ethyl 2-(2,8-dimethyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)-3-methylbutanoate; ethyl 2-(2,8-dimethyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)-3-phenylpropanoate; ethyl 2-(2,8-dimethyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)-3-methoxypropanoate; ethyl 2-(2-methyl-8-phenyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)propanoate; ethyl 2-(8-(4-methoxyphenyl)-2-methyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)propanoate; and ethyl 2-(2-methyl-8-p-tolyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)propanoate.

Certain examples of compounds according to the invention are depicted in Table 3. The compounds depicted may be present as salts even if salts are not depicted and it is understood that the invention embraces all salts, hydrates and solvates of the compounds depicted here, as well as the non-salt, non-hydrate, non-solvate form of the compound, as is well understood by the skilled artisan. It is thus understood that pharmaceutically acceptable salts of compounds according the invention are intended.

TABLE 3 Certain compounds of the invention. Compound No. Name Structure G1 ethyl 2-(2,8-dimethyl-3,4-dihydro-1H-pyrido[4,3- b]indol-5(2H)-yl)propanoate

G2 ethyl 2-(2,8-dimethyl-3,4-dihydro-1H-pyrido[4,3- b]indol-5(2H)-yl)-3-methylbutanoate

G3 ethyl 2-(2,8-dimethyl-3,4-dihydro-1H-pyrido[4,3- b]indol-5(2H)-yl)-3-phenylpropanoate

G4 ethyl 2-(2,8-dimethyl-3,4-dihydro-1H-pyrido[4,3- b]indol-5(2H)-yl)-3-methoxypropanoate

G5 ethyl 2-(2-methyl-8-phenyl-3,4-dihydro-1H- pyrido[4,3-b]indol-5(2H)-yl)propanoate

G6 ethyl 2-(8-(4-methoxyphenyl)-2-methyl-3,4- dihydro-1H-pyrido[4,3-b]indol-5(2H)- yl)propanoate

G7 ethyl 2-(2-methyl-8-p-tolyl-3,4-dihydro-1H- pyrido[4,3-b]indol-5(2H)-yl)propanoate

Pharmaceutical compositions of any of the compounds detailed herein are embraced by this invention. Thus, the invention includes pharmaceutical compositions comprising a compound of the invention or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier or excipient. Pharmaceutical compositions according to the invention may take a form suitable for oral, buccal, parenteral, nasal, topical or rectal administration, or a form suitable for administration by inhalation.

General Description of Biological Assays

The binding properties of compounds disclosed herein to a panel of aminergic G protein-coupled receptors including adrenergic receptors, dopamine receptors, serotonin receptors, histamine receptors and an imidazoline receptor may be determined. Binding properties may be assessed by methods known in the art, such as competitive binding assays. In one variation, compounds are assessed by the binding assays detailed herein. Compounds disclosed herein may also be tested in cell-based assays or in in vivo models for further characterization. In one aspect, compounds disclosed herein are of any formula detailed herein and further display one or more of the following characteristics: inhibition of binding of a ligand to an adrenergic receptor (e.g., α_(1D), α_(2A) and α_(2B)), inhibition of binding of a ligand to a serotonin receptor (e.g., 5-HT_(2A), 5-HT_(2C), 5-HT₆ and 5-HT₇), inhibition of binding of a ligand to a dopamine receptor (e.g., D_(2L)), and inhibition of binding of a ligand to a histamine receptor (e.g., H₁, H₂ and H₃); agonist/antagonist activity to a serotonin receptor (e.g., 5-HT_(2A), 5-HT₆); agonist/antagonist activity to a dopamine receptor (e.g., D_(2L), D_(2S)); agonist/antagonist activity to a histamine receptor (e.g., H₁); activity in a neurite outgrowth assay; efficacy in a preclinical model of memory dysfunction associated with cholinergic hyperfunction; and efficacy in a preclinical model of schizophrenia.

In one variation, inhibition of binding of a ligand to a receptor is measured in the assays described herein. In another variation, inhibition of binding of a ligand is measured in an assay known in the art. In one variation, binding of a ligand to a receptor is inhibited by at least about 80% as determined in a suitable assay known in the art such as the assays described herein. In one variation, binding of a ligand to a receptor is inhibited by greater than about any one of 80%, 85%, 90%, 95%, 100%, or between about 85-95% or between about 90-100% as determined in a suitable assay known in the art such as the assays described herein. In one variation, binding of a ligand to a receptor is inhibited by at least about 80%±20% as determined in an assay known in the art.

In one variation, a compound of the invention inhibits binding of a ligand to at least one receptor and as many as eleven as detailed herein (e.g. α_(1D), α_(2A), α_(2B), 5-HT_(2A), 5-HT_(2C), 5-HT6, 5-HT₇, D_(2L), H₁, H₂, H₃). In one variation, a compound of the invention inhibits binding of a ligand to at least one and as many as eleven receptors detailed herein and further displays agonist or antagonist activity to one or more receptors detailed herein (e.g., serotonin receptor 5-HT_(2A), serotonin receptor 5-HT₆, dopamine receptor D_(2L), and dopamine receptor D_(2S), histamine receptor H₁) as measured in the assays described herein. In one variation, agonist response of serotonin receptor 5-HT_(2A) is inhibited by compounds of the invention by at least about any one of 50%, 50%, 70%, 80%, 90%, 100%, 110%, 120%, 130%, 140%, 150% as determined in a suitable assay such as the assay described herein.

In one variation, a compound of the invention displays the above described neurotransmitter receptor binding profile i.e. inhibits binding of a ligand to at least one receptor and as many as eleven as detailed herein and further stimulates neurite outgrowth, e.g. as measured by the assays described herein. In one variation, a compound of the invention shows activity in neurite outgrowth assays using primary neurons in culture. In another variation, a compound of the invention has activity comparable in magnitude to that of naturally occurring prototypical neurotrophic proteins such as brain derived neurotrophic factor (BDNF) and nerve growth factor (NGF). Notably, neurite outgrowth plays a critical part of new synaptogenesis, which is beneficial for the treatment of neuronal disorders. In one variation, neurite outgrowth is observed with a potency of about 1 μM as measured in a suitable assay known in the art such as the assays described herein. In another variation, neurite outgrowth is observed with a potency of about 500 nM. In a further variation, neurite outgrowth is observed with a potency of about 50 nM. In another variation, neurite outgrowth is observed with a potency of about 5 nM.

In another variation, a compound of the invention inhibits binding of a ligand to at least one receptor and as many as eleven as detailed herein, further displays agonist or antagonist activity to one or more receptors detailed herein and further stimulates neurite outgrowth.

In a further variation, a compound of the invention inhibits binding of a ligand to at least one and as many as eleven receptors as detailed herein and/or display the above described neurotransmitter receptor binding profile and further shows efficacy in a preclinical model of memory dysfunction associated with cholinergic hyperfunction, i.e. shows pro-cognitive effects in a preclinical model of memory dysfunction. In one variation, a compound of the invention is effective in a preclinical model of memory dysfunction associated with cholinergic hypofunction. As H₁ antagonism may contribute to sedation, weight gain and reduced cognition, low affinity (less than about 80% inhibition of binding of Pyrilamine at 1 μM in the assay described herein) for this receptor may be associated with pro-cognitive effects and a more desirable side effect profile. Furthermore, compounds of the invention with increased potency as a 5-HT₆ antagonist may have cognition-enhancing effects as serotonin acting through this receptor may impair memory.

In another variation, a compound of the invention inhibits at least one and as many as eleven receptors as detailed herein, further shows efficacy in a preclinical model of memory dysfunction associated with cholinergic hyperfunction i.e. shows pro-cognitive effects in a preclinical model of memory dysfunction and further displays agonist or antagonist activity to one or more receptors detailed herein.

In a further variation, a compound of the invention inhibits binding of a ligand to at least one and as many as eleven receptors as detailed herein, further shows efficacy in a preclinical model of memory dysfunction associated with cholinergic hyperfunction i.e. shows pro-cognitive effects in a preclinical model of memory dysfunction and further stimulates neurite outgrowth.

In another variation, a compound of the invention inhibits at least one and as many as eleven receptors as detailed herein, further shows efficacy in a preclinical model of memory dysfunction associated with cholinergic hyperfunction i.e. shows pro-cognitive effects in a preclinical model of memory dysfunction, further displays agonist or antagonist activity to one or more receptor detailed herein and further stimulates neurite outgrowth.

In a further variation, a compound of the invention inhibits binding of a ligand to at least one and as many as eleven receptors and further possess anti-psychotic effects as measured in a preclinical model of schizophrenia, i.e., shows efficacy in a preclinical model of schizophrenia.

In another variation, a compound of the invention inhibits binding of a ligand to at least one and as many as eleven receptors, further shows efficacy in a preclinical model of schizophrenia and further displays agonist or antagonist activity to one or more receptors detailed herein.

In a further variation, a compound of the invention inhibits binding of a ligand to at least one and as many as eleven receptors, further shows efficacy in a preclinical model of schizophrenia and further stimulates neurite outgrowth.

In a further variation, a compound of the invention inhibits binding of a ligand to at least one and as many as eleven receptors, further shows efficacy in a preclinical model of memory dysfunction associated with cholinergic hyperfunction and further shows efficacy in a preclinical model of schizophrenia.

In another variation, a compound of the invention inhibits binding of a ligand to at least one and as many as eleven receptors, further shows efficacy in a preclinical model of schizophrenia, further displays agonist or antagonist activity to one or more receptors detailed herein and further shows efficacy in a preclinical model of memory dysfunction associated with cholinergic hyperfunction.

In another variation, a compound of the invention inhibits binding of a ligand to at least one and as many as eleven receptors, further shows efficacy in a preclinical model of schizophrenia, further stimulates neurite outgrowth and further shows efficacy in a preclinical model of memory dysfunction associated with cholinergic hyperfunction.

In a further variation, a compound of the invention inhibits binding to at least one and as many as eleven receptors detailed herein, further displays agonist or antagonist activity to one ore more receptors detailed herein, further stimulates neurite outgrowth and further shows efficacy in a preclinical model of schizophrenia.

In another variation, a compound of the invention inhibits binding of a ligand to at least one and as many as eleven receptors, further shows efficacy in a preclinical model of schizophrenia, further displays agonist or antagonist activity to one or more receptors detailed herein, further stimulates neurite outgrowth and further shows efficacy in a preclinical model of memory dysfunction associated with cholinergic hyperfunction.

In another variation, a compound of the invention stimulates neurite outgrowth. In another variation, a compound of the invention shows efficacy in a preclinical model of schizophrenia and further stimulates neurite outgrowth. In another variation, a compound of the invention stimulates neurite outgrowth and further shows efficacy in a preclinical model of memory dysfunction associated with cholinergic hyperfunction. In another variation, a compound of the invention shows efficacy in a preclinical model of schizophrenia, further stimulates neurite outgrowth and further shows efficacy in a preclinical model of memory dysfunction associated with cholinergic hyperfunction.

In one aspect, compounds of the invention inhibit binding of a ligand to adrenergic receptors α_(1D), α_(2A), α_(2B) and inhibit binding of a ligand to serotonin receptor 5-HT6. In another variation, compounds of the invention inhibit binding of a ligand to adrenergic receptors α_(1D), α_(2A), α_(2B), to serotonin receptor 5-HT₆ and to any one or more of the following receptors: serotonin receptor 5-HT₇, 5-HT_(2A) and 5-HT_(2C). In another variation, compounds of the invention inhibit binding of a ligand to adrenergic receptors α_(1D), α2A, α_(2B), to serotonin receptor 5-HT₆ and to any one or more of the following receptors: serotonin receptor 5-HT₇, 5-HT_(2A) and 5-HT_(2C) and further show weak inhibition of binding of a ligand to histamine receptor H₁ and/or H₂. In one variation, compounds of the invention that also display strong inhibition of binding of a ligand to the serotonin receptor 5-HT₇ are particularly desired. In another variation, compounds of the invention inhibit binding of a ligand to adrenergic receptors α_(1D), α_(2A), α_(2B), to serotonin receptor 5-HT₆ and further show weak inhibition of binding of a ligand to histamine receptor H₁ and/or H₂. Weak inhibition of binding of a ligand to the histamine H₁ receptor is permitted as agonists of this receptor have been implicated in stimulating memory as well as weight gain. In one variation, binding to histamine receptor H₁ is inhibited by less than about 80%. In another variation, binding of a ligand to histamine receptor H₁ is inhibited by less than about any of 75%, 70%, 65%, 60%, 55%, or 50% as determined by a suitable assay known in the art such as the assays described herein.

In another variation, compounds of the invention inhibit binding of a ligand to dopamine receptor D_(2L). In another variation, compounds of the invention inhibit binding of a ligand to dopamine receptor D_(2L) and to serotonin receptor 5-HT_(2A). In another variation, compounds of the invention inhibit binding of a ligand to histamine receptor H₁. In certain aspects, compounds of the invention further show one or more of the following properties: strong inhibition of binding of a ligand to the serotonin 5-HT₇ receptor, strong inhibition of binding of a ligand to the serotonin 5-HT_(2A) receptor, strong inhibition of binding of a ligand to the serotonin 5-HT_(2C) receptor, weak inhibition of binding of a ligand to the histamine H₁ receptor, weak inhibition of binding of ligands to the histamine H₂ receptor, and antagonist activity to serotonin receptor 5-HT_(2A).

In one variation, compounds of the invention show any of the receptor binding aspects detailed herein and further display agonist/antagonist activity to one or more of the following receptors: serotonin receptor 5-HT_(2A), serotonin receptor 5-HT6, dopamine receptor D_(2L), dopamine receptor D_(2S) and histamine receptor H₁. In one variation, compounds of the invention show any of the receptor binding aspects detailed herein and further stimulate neurite outgrowth. In one variation, compounds of the invention show any of the receptor binding aspects detailed herein and further show efficacy in a preclinical model of memory dysfunction associated with cholinergic hyperfunction. In one variation, compounds of the invention show any of the receptor binding aspects detailed herein and further show efficacy in a preclinical model of schizophrenia. In one variation, compounds of the invention show any of the receptor binding aspects detailed herein and further show efficacy in any one or more of agonist/antagonist assays (e.g., to serotonin receptor 5-HT_(2A), 5-HT6, dopamine receptor D_(2L), dopamine receptor D_(2S) and histamine receptor H₁), neurite outgrowth, a preclinical model of memory dysfunction associated with cholinergic hyperfunction and a preclinical model of schizophrenia.

In some aspects, compounds of the invention inhibit binding of a ligand to adrenergic receptors α1D, α2A, α2B, serotonin receptor 5-HT₆ and dopamine receptor D_(2L) by at least about 80% as determined in a suitable assay known in the art such as the assays described herein. In one variation binding is inhibited by at least about 80% as measured in a suitable assay such as the assays described herein. In one variation, binding of a ligand to a receptor is inhibited by greater than about any one of 80%, 85%, 90%, 95%, 100%, or between about 85-95% or about 90-100% as determined in a suitable assay known in the art such as the assays described herein.

In some aspects, compounds of the invention display the above described neurotransmitter receptor binding profile and further show antipsychotic effects. In one variation, a compound of the invention has binding profiles similar to compounds with antipsychotic activity. In another variation, a compound of the invention is effective in a preclinical model of schizophrenia. In addition, compounds of the invention might possess the cognitive enhancing properties of dimebon and thus add to the beneficial pharmacology profile of these antipsychotic molecules. In one variation, compounds of the invention display the above described neurotransmitter receptor binding profile and further show pro-cognitive effects in a preclinical model of memory dysfunction. In another variation, compounds of the invention display the above described neurotransmitter receptor binding profile and do not show pro-cognitive effects in a preclinical model of memory dysfunction.

In one variation, compounds of the invention demonstrate pro-cognitive effects in a preclinical model of memory dysfunction. In a further variation, compounds of the invention possess anti-psychotic effects in a preclinical model of schizophrenia. In a further variation, compounds of the invention demonstrate pro-cognitive effects in a preclinical model of memory dysfunction and further possess anti-psychotic effects in a preclinical model of schizophrenia.

Overview of the Methods

The compounds described herein may be used to treat, prevent, delay the onset and/or delay the development of cognitive disorders, psychotic disorders, neurotransmitter-mediated disorders and/or neuronal disorders in individuals, such as humans. In one aspect, the compounds described herein may be used to treat, prevent, delay the onset and/or delay the development of a cognitive disorder. In another aspect, the compounds described herein may be used to treat, prevent, delay the onset and/or delay the development of a psychotic disorder. In yet another aspect, the compounds described herein may be used to treat, prevent, delay the onset and/or delay the development of a neurotransmitter-mediated disorders disorder. In one embodiment, the neurotransmitter-mediated disorder includes spinal cord injury, diabetic neuropathy, allergic diseases (including food allergies) and diseases involving geroprotective activity such as age-associated hair loss (alopecia), age-associated weight loss and age-associated vision disturbances (cataracts). In another variation, the neurotransmitter-mediated disorder includes spinal cord injury, diabetic neuropathy, fibromyalgia and allergic diseases (including food allergies). In still another embodiment, the neurotransmitter-mediated disorder includes Alzheimer's disease, Parkinson's Disease, autism, Guillain-Barré syndrome, mild cognitive impairment, multiple sclerosis, stroke and traumatic brain injury. In yet another embodiment, the neurotransmitter-mediated disorder includes schizophrenia, anxiety, bipolar disorders, psychosis and depression. In another aspect, the compounds described herein may be used to treat, prevent, delay the onset and/or delay the development of a neuronal disorder. In one aspect, the compounds described herein may also be used to treat, prevent, delay the onset and/or delay the development of cognitive disorders, psychotic disorders, neurotransmitter-mediated disorders and/or neuronal disorders for which the modulation of an aminergic G protein-coupled receptor is believed to be or is beneficial.

The invention also provides methods of improving cognitive functions and/or reducing psychotic effects comprising administering to an individual in need thereof an amount of a compound of the invention or a pharmaceutically acceptable salt thereof effective to improve cognitive functions and/or reduce psychotic effects.

The invention also provides methods of stimulating neurite outgrowth and/or promoting neurogenesis and/or enhancing neurotrophic effects in an individual comprising administering to an individual in need thereof an amount of a compound of the invention or a pharmaceutically acceptable salt thereof effective to stimulate neurite outgrowth and/or to promote neurogenesis and/or to enhance neurotrophic effects.

The invention further encompasses methods of modulating an aminergic G protein-coupled receptor comprising administering to an individual in need thereof an amount of a compound of the invention or a pharmaceutically acceptable salt thereof effective to modulate an aminergic G protein-coupled receptor.

It is to be understood that methods described herein also encompass methods of administering compositions comprising the compounds of the invention.

Methods for Treating, Preventing, Delaying the Onset, and/or Delaying the Development Cognitive Disorders, Psychotic Disorders, Neurotransmitter-mediated Disorders and/or Neuronal Disorders

In one aspect, the invention provides methods for treating, preventing, delaying the onset, and/or delaying the development of cognitive disorders, psychotic disorders, neurotransmitter-mediated disorders and/or neuronal disorders for which the modulation of an aminergic G protein-coupled receptor is believed to be or is beneficial, the method comprising administering to an individual in need thereof a compound of the invention. In some variations, modulation of adrenergic receptor α_(1D), α_(2A), α_(2B), serotonin receptor 5-HT_(2A), 5-HT6, 5HT7, histamine receptor H₁ and/or H₂ is expected to be or is beneficial for the cognitive disorders, psychotic disorders, neurotransmitter-mediated disorders and/or neuronal disorders. In some variations, modulation of adrenergic receptor α_(1D), α_(2A), α_(2B) and a serotonin receptor 5-HT₆ receptor is expected to be or is beneficial for the cognitive disorders, psychotic disorders, neurotransmitter-mediated disorders and/or neuronal disorders. In some variations, modulation of adrenergic receptor α_(1D), α_(2A), α_(2B), and a serotonin receptor 5-HT₆ receptor and modulation of one or more of the following receptors serotonin 5-HT₇, 5-HT_(2A), 5-HT_(2C) and histamine H₁ and H₂ is expected to be or is beneficial for the cognitive disorders, psychotic disorders, neurotransmitter-mediated disorders and/or neuronal disorders. In some variations, modulation of dopamine receptor D_(2L) is expected to be or is beneficial for the cognitive disorders, psychotic disorders, neurotransmitter-mediated disorders and/or neuronal disorders. In certain variations, modulation of a dopamine D_(2L) receptor and serotonin receptor 5-HT_(2A) is expected to be or is beneficial for the cognitive disorders, psychotic disorders, neurotransmitter-mediated disorders and/or neuronal disorders. In some variations, the cognitive disorders, psychotic disorders, neurotransmitter-mediated disorders and/or neuronal disorders are treated, prevented and/or their onset or development is delayed by administering a compound of the invention.

Methods to Improve Cognitive Functions and/or Reduce Psychotic Effects

The invention provides methods for improving cognitive functions by administering a compound of the invention to an individual in need thereof. In some variations, modulation of one or more of adrenergic receptor α_(1D), α_(2A), α_(2B), serotonin receptor 5-HT_(2A), 5-HT6, 5HT7, histamine receptor H₁ and/or H₂ is desirable or expected to be desirable to improve cognitive functions. In some variations modulation of α_(1D), α_(2A), α_(2B) adrenergic receptors and a serotonin 5-HT₆ receptor is desirable or expected to be desirable to improve cognitive functions. In some variations, modulation of α_(1D), α_(2A), α_(2B) adrenergic receptors and serotonin receptor 5-HT₆ and modulation of one or more of the following receptors: serotonin receptor 5-HT₇, 5-HT_(2A), 5-HT_(2C) and histamine receptor H₁ and H₂, is desirable or expected to be desirable to improve cognitive functions. In another aspect, the invention encompasses methods to reduce psychotic effects by administering a compound of the invention to an individual in need thereof. In some embodiments, modulation of a dopamine D_(2L) receptor is expected to be or is desirable to reduce psychotic effects. In some embodiments, modulation of a dopamine D_(2L) receptor and a serotonin 5-HT_(2A) receptor is expected to be or is desirable to reduce psychotic effects. In some variations, a compound of the invention is administered to an individual in need thereof.

Methods to Stimulate Neurite Outgrowth, Promote Neurogenesis and/or Enhance Neurotrophic Effects

In a further aspect, the invention provides methods of stimulating neurite outgrowth and/or enhancing neurogenesis and/or enhancing neurotrophic effects comprising administering a compound of the invention or pharmaceutically acceptable salt thereof under conditions sufficient to stimulate neurite outgrowth and/or to enhance neurogenesis and/or enhance neurotrophic effects to an individual in need thereof. In some variations, a compound of the invention stimulates neurite outgrowth at a potency of about 1 μM as measured in a suitable assay such as the assays described herein. In some variations, a compound of the invention stimulates neurite outgrowth at a potency of about 500 nM as measured in a suitable assay such as the assays described herein. In some variations, a compound of the invention stimulates neurite outgrowth at a potency of about 50 nM as measured in a suitable assay such as the assays described herein. In some variations, a compound of the invention stimulates neurite outgrowth at a potency of about 5 nM as measured in a suitable assay such as the assays described herein.

Methods to Modulate an Aminergic G Protein-Coupled Receptor

The invention further contemplates methods for modulating the activity of an aminergic G-protein-coupled receptor comprising administering a compound of the invention or pharmaceutically acceptable salt thereof under conditions sufficient to modulate the activity of an aminergic G protein-coupled receptor. In some variations, the aminergic G protein-coupled receptor is a α_(1D), α_(2A), α_(2B) adrenergic receptor and a serotonin 5-HT₆ receptor. In some variations, the aminergic G protein-coupled receptor is a α_(1D), α_(2A), α_(2B) adrenergic receptor and a serotonin 5-HT₆ and 5-HT₇ receptor. In some variations, the aminergic G protein-coupled receptor is a α_(1D), α_(2A), α_(2B) adrenergic receptor, a serotonin 5-HT₆ and one or more of the following receptors: serotonin 5-HT-7, 5-HT_(2A) and 5-HT_(2C) and histamine H₁ and H₂ receptor. In some variations, the aminergic G protein-coupled receptor is a dopamine D_(2L) receptor. In some variations, the aminergic G protein-coupled receptor is a dopamine D_(2L) receptor and a serotonin 5-HT_(2A) receptor. In some variations, the aminergic G protein-coupled receptor is a histamine H₁ receptor.

General Synthetic Methods

The compounds of the invention may be prepared by a number of processes as generally described below and more specifically in the Examples hereinafter. In the following process descriptions, the symbols when used in the formulae depicted are to be understood to represent those groups described above in relation to formula (I) or a variation thereof unless otherwise indicated.

Where it is desired to obtain a particular enantiomer of a compound, this may be accomplished from a corresponding mixture of enantiomers using any suitable conventional procedure for separating or resolving enantiomers. Thus, for example, diastereomeric derivatives may be produced by reaction of a mixture of enantiomers, e.g. a racemate, and an appropriate chiral compound. The diastereomers may then be separated by any convenient means, for example by crystallization and the desired enantiomer recovered. In another resolution process, a racemate may be separated using chiral High Performance Liquid Chromatography. Alternatively, if desired a particular enantiomer may be obtained by using an appropriate chiral intermediate in one of the processes described.

Chromatography, recrystallization and other conventional separation procedures may also be used with intermediates or final products where it is desired to obtain a particular isomer of a compound or to otherwise purify a product of a reaction.

The following abbreviations are used herein: thin layer chromatography (TLC); Hour (h); Ethanol (EtOH); dimethylsulfoxide (DMSO); N,N-dimethylformamide (DMF); trifluoroacetic acid (TFA); teterahydrofuran (THF); Normal (N); aqueous (aq.); methanol (MeOH); dichloromethane (DCM); Retention factor (Rf).

Compounds made by General Methods 1 and 8 may also be used as intermediates for the synthesis of other compounds of the invention.

General Method 1

Compound A (1 equiv.), triethylamine (3 equiv) and compound B (1 equiv.) are dissolved in EtOH and stirred at 25° C. for 1 h and then at 90° C. for 3 h after which the contents are cooled to 25° C. and evaporated to dryness to obtain crude C. The residue is acidified with ethanolic HCl and the volatiles are removed under reduced pressure. Ethanol is added followed by compound D (1 to 1.5 equiv) and the contents are heated at 90° C. for additional 16 h. Solvent is removed in vacuo. The remaining residue is diluted with ethyl acetate and washed with saturated aq. NaHCO₃. The aqueous layer is extracted twice with ethyl acetate and the combined organic layer is dried over Na₂SO₄, and concentrated. The resulting crude product is purified by silica gel chromatography (100-200 mesh or 230-400 mesh) using methanol-dichloromethane gradient, by neutral alumina using ethyl acetate-hexane gradient, and/or by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 mL). Similar synthetic details may be employed for compounds made according to Scheme 1-B. This procedure is exemplified by the synthesis of compounds CD11, CD17, CD19, CD27 and CD29.

General Method 2

A mixture of compounds E (1 equiv.) and F (neat or aqueous, 10-25 folds w/v) is heated at 100-120° C. for 3-4 h after which the reaction mixture is evaporated to dryness. The resulting crude product is purified by silica gel chromatography (100-200 mesh or 230-400 mesh) using methanol-dichloromethane gradient, by neutral alumina using ethyl acetate-hexane gradient, and/or by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 mL). Similar synthetic details may be employed for compounds made according to Scheme 2-B.

General Method 3

General methods according to Schemes 3-A and 3-B are exemplified below for the synthesis of CD63.

The reaction of described above for 4-chlorophenylhydrazine, which can be extended to any appropriately substituted phenyl hydrazine (such as H or H-1), with ethyl bromo (or chloro)acetate under appropriate alkylating conditions results in the formation of the internally substituted hydrazine (I38) The reaction of (I38) with N-methyl-4-piperidone results in the formation of the carboline (II38). The hydrolysis of (II38) gives the acid 38. Similar synthetic details may be employed in the reaction according to Scheme 3-A or 3-B.

General Method 4

General methods according to Schemes 4-A and 4-B are exemplified below for the synthesis of CD55.

The reaction of 4-chlorophenylhydrazine, which can be extended to any appropriately substituted phenyl hydrazine (such as H-2), with ethyl 3-bromo(or chloro)propionate under appropriate alkylating conditions results in the formation of the internally substituted hydrazine (III39). The reaction of (III39) with N-methyl-4-piperidone results in the formation of the carboline (IV39). The hydrolysis of (IV39) gives the acid (39). Similar synthetic details may be employed in the reaction according to Scheme 4-A.

General Method 5

Certain compounds of the invention are synthesized according to Schemes 5-A and 5-B as exemplified by the methods according to Schemes 5-C and 5-D. Dichloromethan can be used as the solvent in place of or in addition to DMF as shown in Schemes 5-A to 5-D. For example, dichloromethane is used as solvent in the syntheses of compounds CD13 and CD15.

The carboxylic acids (exemplified above for 3-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanoic acid) of the general structure described above can be treated with DCC/DMAP in an appropriate solvent, such as dimethylformamide or methylene chloride followed by treatment with a desired alcohol (R_(a)—OH) to provide the corresponding esters. Isolation and purification of these esters can be carried out using standard work up and normal phase or reverse phase chromatographic methods.

General Method 6

Certain compounds of the invention are synthesized according to Schemes 6-A and 6-B as exemplified by the methods according to Schemes 6-C and 6-D. Dichloromethan can be used as the solvent in place of or in addition to DMF as shown in Schemes 6-A to 6-D. For example, dichloromethane is used as solvent in the syntheses of compound CD25.

The carboxylic acids (exemplified above for 3-(2,8-dimethyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)propanoic acid) of the general structure described above can be treated with DCC/DMAP in an appropriate solvent, such as dimethylformamide or methylene chloride followed by treatment with a desired amine (R_(a)—NH₂) to provide the corresponding amides. Isolation and purification of these amides can be carried out using standard work up and normal phase or reverse phase chromatographic methods.

General Method 7

General method according to Scheme 7-A is exemplified by the synthesis of CD33-CD35 (esters) and CD36-CD38 (amines).

The reaction of 4-pyridylhydrazine with ethyl 4-bromo(or chloro)butanoate under appropriate alkylating conditions results in the formation of the internally substituted hydrazine (i) The reaction of (i) with N-methyl-4-piperidone results in the formation of the carboline (ii). The hydrolysis of (ii) gives the acid (iii). The carboxylic acids, including (iii) can be treated with DCC/DMAP in an appropriate solvent, such as dimethylformamide or methylene chloride followed by treatment with (a) a desired alcohol (R—OH) to provide the corresponding esters, or (b) a desired amine (R_(a)—NH₂) to provide the corresponding amides. Isolation and purification of these esters can be carried out using standard work up and normal phase or reverse phase chromatographic methods.

General Method 8

General method according to Scheme 8-A is exemplified by the synthesis of CD39-CD41.

The reaction of a 4-pyridylhydrazine with 3-bromo(or chloro)propionitrile under appropriate alkylating conditions results in the formation of the internally substituted hydrazine (V) which upon treatment with N-methyl-4-piperidone and reduction of the corresponding carboline results in the formation of the amine (42). The conversion of the amine (42) to the amides described above can be carried out using standard peptide coupling conditions in an appropriate solvent, such as dimethylformamide or methylene chloride followed by treatment with desired acids, to provide the corresponding amides. Isolation and purification of these amides can be carried out using standard work up and normal phase or reverse phase chromatographic methods.

The reaction of a 4-pyridylhydrazine with bromo(or chloro)acetonitrile under appropriate alkylating conditions results in the formation of the internally substituted hydrazine (VI) which upon treatment with N-methyl-4-piperidone and reduction of the corresponding carboline results in the formation of the amine (43). The conversion of the amine (43) to the amides described above can be carried out using standard peptide coupling conditions in an appropriate solvent, such as dimethylformamide or methylene chloride followed by treatment with desired acids, to provide the corresponding amides. Isolation and purification of these amides can be carried out using standard work up and normal phase or reverse phase chromatographic methods.

General Method 9.

Certain compounds of the invention are synthesized using acid chloride intermediates as shown in Scheme 9. This general method is exemplified by the syntheses of compounds CD16, CD18 and CD20-CD22.

General Method 10.

Certain compounds of the invention are synthesized using an acid amine transfer method as shown in Scheme 10. This general method is exemplified by the syntheses of compounds CD2, CD3, CD5, CD23 and CD24.

General Method 11.

Certain compounds of the invention are synthesized using a EDCI as a coupling reagent as shown in Scheme. Solvents for the reaction, e.g. DMF or dichlormethane can be selected by one skilled in the art, for example, based on choice of starting materials. This general method is exemplified by the syntheses of compounds CD4, CD12, CD14, CD26, CD30, CD31 and CD54.

General Method 12.

Compounds of structure 103 can be synthesized using the general synthetic protocol outlined in General Method 1. Appropriately substituted compounds of structure 101, wherein R² and R³ are as described hereinabove, can be reacted under standard alkylating conditions with appropriately substituted compounds of structure 102, wherein R¹ and R⁴ are as described hereinabove and X is a halogen selected from Cl, Br, and I, to give compounds of structure 103.

In one variation, sodium hydride (260 mmol) is added to a solution of 101 in DMF (150 ml) with stirring and cooling. After 30 minutes a solution of 102 (260 mmol) in DMF (20 ml) is added dropwise over 10-15 minutes to the reaction mixture. Obtained mixture is stirred at 70° C. for 10 h. The reaction mixture is evaporated to dryness under vacuum; the residue is poured into ice water (100 ml) and is extracted with methylene chloride (3×100 ml). The organic extract is dried with anhydrous sodium sulfate, the solvent is evaporated under vacuum, and the residue is recrystallized from benzene or it is chromatographed on dry column in the system petroleum ether-ethyl acetate with concentration gradient up to 15% of the latter to obtain 103.

General Method 13a.

Compounds of structure 103 can also be synthesized using the general synthetic protocol outlined in General Method 2a. Appropriately substituted compounds of structure 201, wherein R² is as described hereinabove, may be reacted under standard alkylating conditions with appropriately substituted compounds of structure 102, wherein R¹ and R⁴ are described hereinabove and X is selected from Cl, Br, and I, to give compounds of structure 202. Reaction of compounds of structure 202 under standard Fischer indole synthesis conditions with compounds of structure 203, wherein R³ is as described hereinabove, gives compounds of structure 103.

General Method 13b.

In another variation, the compounds of structure 103 can be synthesized according to the general synthetic protocol outlined in General Method 2b. Solution of aniline (10 mmol), ester of 102 (10 mmol) and diisopropylethylamine (10 mmol) in THF (40 ml) is reflux for 24 h. The reaction mixture is poured into ice water (100 ml) and is extracted with methylene chloride (4×50 ml). The organic extract is dried with anhydrous sodium sulfate, the solvent is evaporated under vacuum, and the residue is dissolved in ethanol and an excess of hydrogen chloride solution in ether is added. The volatile components are removed under vacuum, and the residue is recrystallized from ethanol-ether mixture to provide a compound of structure 200.

Hydrochloride of 200 (5.2 mmol) is added all at once with cooling and vigorous stiffing to 50 ml of cold solution of potassium hydroxide (5.2 mmol) in water. Amine is extracted with ether (3×50 ml), is washed with water and a saturated sodium chloride solution, and the extract is dried with anhydrous sodium sulfate. The solvent is removed at reduced pressure, the residue is dissolved in anhydrous THF (10 ml), and 14% solution of ethyl nitrite in alcohol (˜7.2 mmol) is added in portions with cooling and stirring to the solution obtained. The reaction mixture is held for 12 h at room temperature in the dark. The volatile components are removed under vacuum with bath temperature of 40° C., and a compound of formula 201 is obtained. This compound is used in later conversions without additional purification.

Concentrated HCl (72 ml) and (in portions with vigorous stiffing) zinc dust (75 mmol) are added to a solution of nitrosamine of 201 (9 mmol) in absolute methanol (100 ml) with cooling down to −80° C. in argon atmosphere. The reaction mixture is stirred vigorously for 6-8 h at temperature from −80° C. to −70° C. in argon atmosphere. The completeness of reduction is monitored by TLC. The excess of zinc is filtered off, the residue is washed with methanol (20 ml), the filtrate is evaporated under vacuum at room temperature down to a volume of ˜20 ml, is poured into ice water (100 ml) and is made alkaline by adding of 24% aqueous solution of ammonia (20 ml). This is extracted with methylene chloride (4×50 ml), the extract is washed with saturated sodium chloride solution (30 ml) and is dried with anhydrous sodium sulfate. After removing the solvent under vacuum, a compound of the formula 202 is obtained. This substance is used without additional purification.

Compound of structure 203 (4 mmol) and a catalytic amount of p-toluenesulfonic acid are added to a solution of compound 202 (4 mmol) in benzene (10 ml), and the mixture is boiled for 8 h with a Dean and Stark still head. The formation of hydrazone is confirmed by LC-MS. Benzene is removed under reduced pressure, the residue is dissolved in toluene (40 ml), Amberlist 15 (3 g) is added, and the mixture is stirred vigorously for 3 h at 90-100° C. The resin is filtered of, washed with ethyl acetate (60 ml), the filtrate is evaporated in vacuum, and the residue is chromatographed on a column of silica gel in the system petroleum ether-ethyl acetate with concentration gradient up to 15% of the latter, to provide a compound of the formula 103.

Compounds G1-G7 are synthesized using General Methods 12, 13a or 13b, or applicable general methods and synthetic procedures described herein. Compound 18 (CD19) is prepared according to General Method 1. Compounds 55 (CD65) and 58 (CD69) are prepared according to General Method 6. Compound 57 (CD67) is prepared according to General Method 8 where X⁹ is CR⁴.

The methods detailed above may be adapted as known by those of skill in the art. Particular examples of each General Method are provided in the Examples below.

The following Examples are provided to illustrate but not limit the invention.

All references disclosed herein are incorporated by reference in their entireties.

EXAMPLES Example 1 Preparation of ethyl 3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanoate (CD1)

Preparation of the title compound was carried out according to General Method 1. p-Tolylhydrazine hydrochloride (20 g, 126 mmol), ethyl 3-bromopropionate (22.8 g, 126 mmol) and triethylamine (38.1 g, 378 mmol) in ethanol (200 ml) were stirred at 25° C. for 1 h after which the contents were heated at 90° C. for 3 h. The contents were cooled to 25° C. and evaporated to dryness. The residue was acidified with ethanolic HCl and the volatiles were removed under reduced pressure. Ethanol (200 mL) was added followed by N-methyl-4-piperidone hydrochloride (2.87 g, 18.9 mmol). Heating was continued at 90° C. for 16 h. The contents were concentrated in vacuo, basified by adding saturated aqueous NaHCO₃, and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated. The crude product was purified by chromatography on neutral alumina using methanol-dichloromethane gradient to obtain 1.5 g of ethyl 3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanoate.

Example 2 Preparation of ethyl 4-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)butanoate (CD6)

Preparation of the title compound was carried out according to General Method 1 by using p-Tolylhydrazine hydrochloride (600 mg, 3.7 mmol), ethyl-4-chlorobutyrate (0.54 ml, 3.7 mmol), triethylamine (1.5 ml, 11.3 mmol) and N-methyl-4-piperidone hydrochloride (0.563 g, 3.7 mmol) in ethanol (10 ml) to obtain 130 mg of ethyl 4-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)butanoate after purification on silica gel (230-400 mesh) chromatography eluting with methanol-dichloromethane gradient. The free base was converted into its oxalate salt by treatment of oxalic acid (1 equiv) in anhydrous THF.

Example 3 Preparation of ethyl 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetate (CD11)

Preparation of the title compound was carried out according to General Method 1 by using

4-chlorophenylhydrazine hydrochloride (5 g, 27.9 mmol), ethyl bromoacetate (4.6 g, 27.9 mmol), triethylamine (11.6 mL, 83.2 mmol) and N-methyl-4-piperidone hydrochloride (5.2 g, 34.9 mmol) in ethanol (50 ml) to obtain 1.3 g of ethyl 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetate after purification on neutral alumina chromatography eluting with dichloromethane-hexane gradient.

Example 4 Preparation of ethyl 3-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanoate (CD59)

Preparation of the title compound was carried out according to General Method 1 by using 4-chlorophenylhydrazine hydrochloride (10 g, 55 mmol), ethyl 3-bromopropionate (7.2 mL, 55 mmol), triethylamine (23 mL, 165 mmol) and N-methyl-4-piperidone hydrochloride (8.3 g, 55 mmol) in ethanol (100 ml) to obtain 1.4 g of ethyl 3-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanoate after purification on neutral alumina chromatography eluting with dichloromethane-hexane gradient.

Example 5 Preparation of 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetonitrile (CD61)

Preparation of the title compound was carried out according to General Method 8 by using p-tolylhydrazine hydrochloride (10 g, 63 mmol), bromo acetonitrile (7.56 ml, 63 mmol), triethylamine (19.1 g, 189 mmol) and N-methyl-4-piperidone hydrochloride (2.54 g, 17 mmol) in ethanol (30 ml) to obtain 1.8 g of 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetonitrile after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient. The TFA salt of this material was obtained by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 mL).

Example 6 Preparation of 2,2,2-trichloroethyl 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethylcarbamate (CD9)

Preparation of the title compound was carried out using p-tolylhydrazine hydrochloride (396 mg, 2.5 mmol), 2,2,2-trichloroethyl 2-bromoethylcarbamate (750 mg, 2.5 mmol), triethylamine (1 ml, 7.4 mmol) and N-methyl-4-piperidone hydrochloride (394 mg, 2.6 mmol) in ethanol-HCl (15 ml) to obtain 160 mg of 2,2,2-trichloroethyl 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethylcarbamate as TFA salt after purification on silica gel (230-400 mesh) chromatography eluting with methanol-dichloromethane gradient followed by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile,

Gradient: 10% B to 80% B in 30 min, injection vol. 5 mL).

Example 7 Preparation of N-(4-fluorophenyl)-3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanamide (CD50)

Preparation of the title compound was carried out using p-tolylhydrazine hydrochloride (1.1 g, 7.4 mmol), 3-chloro-N-(4-fluorophenyl)propanamide (1.5 g, 7.4 mmol), triethylamine (2.2 g, 22.3 mmol) and N-methyl-4-piperidone hydrochloride (1.1 g, 7.4 mmol) in ethanol-HCl (12 ml) to obtain N-(4-fluorophenyl)-3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)prop an amide as TFA salt after purification on silica gel (230-400 mesh) chromatography eluting with methanol-dichloromethane gradient followed by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 mL).

Example 8 Preparation of 3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)-N-methylpropanamide (CD2)

A mixture of ethyl 3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanoate (100 mg, 0.33 mmol) and methyl amine (40% aq, 2.5 ml) was heated at 100-120° C. for 3-4 h. The reaction mixture was evaporated to dryness and the residue was purified by on neutral alumina chromatography eluting with methanol-dichloromethane gradient to obtain 10 mg of 3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)-N-methylpropanamide.

Example 9 Preparation of N-ethyl-3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanamide (CD3)

A mixture of ethyl 3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanoate (100 mg, 0.33 mmol) and ethyl amine (40% aq, 2.5 ml) was heated at 100-120° C. for 3-4 h to obtain 19 mg of N-ethyl-3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanamide after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient.

Example 10 Preparation of N-cyclopentyl-3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanamide (CD5)

A mixture of ethyl 3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanoate (100 mg, 0.33 mmol) and cyclopentylamine (1 ml, 10 mmol) was heated at 100-120° C. for 3-4 h to obtain 17 mg of N-cyclopentyl-3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanamide after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient.

Example 11 Preparation of N-ethyl-4-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)butanamide (CD7)

Ethyl 4-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)butanoate (80 mg, 0.2 mmol) was stirred with ethylamine (0.8 ml) at 100-120° C. for 3-4 h to obtain 40 mg of N-ethyl-4-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)butanamide after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient.

Example 12 Preparation of 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethanamine (CD62)

2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetonitrile (500 mg, 2 mmol) was treated with diisobutylaluminum hydride (6.2 ml, 6.2 mmol) in toluene (10 ml) at 80° C. to obtain 250 mg of 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethanamine after purification on silica gel (230-400 mesh) chromatography eluting with methanol-dichloromethane gradient.

Example 13 Preparation of tert-butyl 3-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethylcarbamoyl)piperidine-1-carboxylate (CD8)

2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethanamine (100 mg, 0.4 mmol) was mixed with EDCI (78 mg, 0.4 mmol) and N-Boc-(S)-nipecotic acid (94 mg, 0.4 mmol) in dichloromethane (3 ml) and the reaction mixture was stirred for 16 h to obtain tert-butyl 3-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethylcarbamoyl)piperidine-1-carboxylate as TFA salt after purification by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 mL).

Example 14 Preparation of N-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethyl)piperidine-3-carboxamide (CD10)

tert-butyl 3-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethylcarbamoyl)piperidine-1-carboxylate (40 mg, 0.08 mmol) was stirred with trifluoroacetic acid (0.1 mL) in dichloromethane (2 ml) to obtain 10 mg of N-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethyl)piperidine-3-carboxamide as di-TFA salt after purification by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 mL).

Example 14A Preparation of Compound 54 (CD64)

Example 14B Preparation of Compound 56 (CD66)

Example 15 Preparation of 3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanoic acid (CD47)

A mixture of ethyl 3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanoate (100 mg, 0.33 mmol) (1.5 g) and NaOH (3N, 30 ml) in ethanol (30 ml) was stirred at 50° C. for 3 h after which it was cooled to RT and neutralized with conc. HCl. The solvent was removed under reduced pressure to obtain crude 3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanoic acid.

Example 16 Preparation of CD63

The reaction described above for 4-chlorophenylhydrazine, which can be extended to any appropriately substituted phenylhydrazine, with ethyl bromo(or chloro)acetate under appropriate alkylating conditions results in the formation of the internally substituted hydrazine (I). The reaction of (I) with N-methyl-4-piperidone results in the formation of the carboline (II). The hydrolysis of (II) gives the acid 38.

Example 17 Preparation of CD23-CD27 and CD54

The carboxylic acids (exemplified above for 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetic acid) of the general structure described above can be treated with DCC/DMAP in an appropriate solvent, such as dimethylformamide or methylene chloride followed by treatment with a desired amine (R_(a)—NH₂) to provide the corresponding amides. Isolation and purification of these amides can be carried out using standard work up and normal phase or reverse phase chromatographic methods.

Example 18 Preparation of CD2-CD5 and CD29-CD31

The carboxylic acids (exemplified above for 3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanoic acid of the general structure described above can be treated with DCC/DMAP in an appropriate solvent, such as dimethylformamide or methylene chloride followed by treatment with a desired amine (R_(a)—NH₂) to provide the corresponding amides. Isolation and purification of these amides can be carried out using standard work up and normal phase or reverse phase chromatographic methods.

Example 19 Preparation of CD33, CD34 and CD35

The reaction of a 4-pyridylhydrazine with ethyl 4-bromo(or chloro)butanoate under appropriate alkylating conditions results in the formation of the internally substituted hydrazine (i) The reaction of (i) with N-methyl-4-piperidone results in the formation of the carboline (ii). The hydrolysis of (ii) gives the acid (iii). The carboxylic acids, including (iii) can be treated with DCC/DMAP in an appropriate solvent, such as dimethylformamide or methylene chloride followed by treatment with a desired alcohol (R—OH) to provide the corresponding esters. Isolation and purification of these esters can be carried out using standard work up and normal phase or reverse phase chromatographic methods.

Example 20 Preparation of CD36, CD37 and CD38

The reaction of a 4-pyridylhydrazine with ethyl 4-bromo(or chloro)butanoate under appropriate alkylating conditions results in the formation of the internally substituted hydrazine (i). The reaction of (i) with N-methyl-4-piperidone results in the formation of the carboline (ii). The hydrolysis of (ii) gives the acid (iii). The carboxylic acids, including (iii) can be treated with DCC/DMAP in an appropriate solvent, such as dimethylformamide or methylene chloride followed by treatment with a desired amine (R_(a)—NH₂) to provide the corresponding amides. Isolation and purification of these amides can be carried out using standard work up and normal phase or reverse phase chromatographic methods.

Example 21 Preparation of CD39, CD40 and CD41

The reaction of a 4-pyridylhydrazine with 3-bromo(or chloro)propionitrile under appropriate alkylating conditions results in the formation of the internally substituted hydrazine (V) which upon treatment with N-methyl-4-piperidone and reduction of the corresponding carboline results in the formation of the amine (CD68). The conversion of the amine (CD68) to the amides described above can be carried out using standard peptide coupling conditions in an appropriate solvent, such as dimethylformamide or methylene chloride followed by treatment with desired acids, to provide the corresponding amides. Isolation and purification of these amides can be carried out using standard work up and normal phase or reverse phase chromatographic methods.

Example 22 Preparation of CD42, CD43, CD44 and CD45

The reaction of a 4-pyridylhydrazine with bromo(or chloro) acetonitrile under appropriate alkylating conditions results in the formation of the internally substituted hydrazine (VI) which upon treatment with N-methyl-4-piperidone and reduction of the corresponding carboline results in the formation of the amine (CD70). The conversion of the amine (CD70) to the amides described above can be carried out using standard peptide coupling conditions in an appropriate solvent, such as dimethylformamide or methylene chloride followed by treatment with desired acids, to provide the corresponding amides. Isolation and purification of these amides can be carried out using standard work up and normal phase or reverse phase chromatographic methods.

Example 23 Preparation of CD46

A mixture of ethyl 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetate and NaOH in ethanol was stirred at 50° C. for 3 h after which it was cooled to RT and neutralized with conc. HCl. The solvent was removed under reduced pressure to obtain crude 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetic acid.

Example 24 Preparation of CD51

A mixture of ethyl 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetate (100 mg) and dimethylamine (1 ml) was heated at 120° C. for 15 h to obtain 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)-N,N-dimethylacetamide after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient. The free base was converted into its oxalate salt by treatment of oxalic acid (1 equiv) in anhydrous THF.

Example 25 Preparation of CD17

4-Chlorophenylhydrazine hydrochloride, ethyl 3-bromopropionate and triethylamine in ethanol were stirred at 25° C. for 1 h after which the contents were heated at 90° C. for 3 h. The contents were cooled to 25° C. and evaporated to dryness. The residue was acidified with ethanolic HCl and the volatiles were removed under reduced pressure. Ethanol was added followed by N-methyl-4-piperidone hydrochloride. Heating was continued at 90° C. for 16 h. The contents were concentrated in vacuo, basified by adding saturated aqueous NaHCO3, and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated. The crude product was purified by chromatography on neutral alumina using methanol-dichloromethane gradient to obtain ethyl 3-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanoate.

Example 26 Preparation of CD52 and CD60

A mixture of ethyl 3-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanoate (CD17) (100 mg) and dimethylamine (1 ml) was heated at 120° C. for 15 h to obtain 3-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)-N,N-dimethylpropanamide (CD52) after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient. The free base was converted into its HCl salt by treatment of ethanol-HCl.

Compound CD60 is prepared according to the process described herein using appropriately substituted reagents.

Example 27 Preparation of CD57

Preparation of the title compound was carried out according by using p-tolylhydrazine hydrochloride, ethyl bromoacetate, triethylamine and N-methyl-4-piperidone hydrochloride in ethanol to obtain ethyl 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetate after purification on neutral alumina chromatography eluting with dichloromethane-hexane gradient.

Example 28 Preparation of CD58

A mixture of ethyl 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-h]indol-5-yl)acetate and NaOH in ethanol was stirred at 50° C. for 3 h after which it was cooled to RT and neutralized with conc. HCl. The solvent was removed under reduced pressure to obtain crude 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-h]indol-5-yl)acetic acid.

Example 29 Preparation of CD23

A mixture of ethyl 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetate (100 mg) and ethylamine (1 ml) was heated at 120° C. for 15 h to obtain N-ethyl-2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetamide (CD23) after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient. The free base was converted into its oxalate salt by treatment of oxalic acid (1 equiv) in anhydrous THF.

Example 30 Preparation of CD26

2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetic acid (CD58) was mixed with EDCI and benzylamine and the reaction mixture was stirred for 16 h to obtain N-benzyl-2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetamide after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient. The free base was converted into its oxalate salt by treatment of oxalic acid (1 equiv) in anhydrous THF.

Example 31 Preparation of CD28

A mixture of ethyl 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetate (100 mg) and cyclopentylamine (1 ml) was heated at 120° C. for 15 h to obtain 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)-N-cyclopentylacetamide after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient. The free base was converted into its oxalate salt by treatment of oxalic acid (1 equiv) in anhydrous THF.

Example 32 Preparation of CD53

2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethanamine was mixed with EDCI and pyridine-4-carboxylic acid in dichloromethane and the reaction mixture was stirred for 16 h to obtain N-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethyl)isonicotinamide as TFA salt after purification by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05

Example 33 Preparation of CD54

2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetic acid (CD58) was mixed with EDCI and 4-fluoroaniline and the reaction mixture was stirred for 16 h to obtain N-(4-fluorophenyl)-2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetamide after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient. The free base was converted into its oxalate salt by treatment of oxalic acid (1 equiv) in anhydrous THF.

Example 34 Preparation of CD12

2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetic acid was mixed with EDCI and isopropanol and the reaction mixture was stirred for 16 h to obtain isopropyl 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetate after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient. The free base was converted into its oxalate salt by treatment of oxalic acid (1 equiv) in anhydrous THF.

Example 35 Preparation of CD30

3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanoic acid was mixed with EDCI and aniline in dichloromethane and the reaction mixture was stirred for 16 h to obtain CD30 after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient. The free base was converted into its oxalate salt by treatment of oxalic acid (1 equiv) in anhydrous THF.

Example 36 Preparation of CD32

A mixture of ethyl 3-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanoate (CD17) (100 mg) and cyclopentylamine (1 ml) was heated at 120° C. for 15 h to obtain 3-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)-N-cyclopentylpropanamide

(CD32) after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient. The free base was converted into its oxalate salt by treatment of oxalic acid (1 equiv) in anhydrous THF.

Example 37 Preparation of CD55

A mixture of ethyl 3-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanoate (CD17) and NaOH in ethanol was stirred at 50° C. for 3 h after which it was cooled to RT and neutralized with conc. HCl. The solvent was removed under reduced pressure to obtain crude 3-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanoic acid.

Example 38 Preparation of CD56

2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetic acid was mixed with EDCI and 1-butanol and the reaction mixture was stirred for 16 h to obtain butyl 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetate after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient. The free base was converted into its oxalate salt by treatment of oxalic acid (1 equiv) in anhydrous THF.

Example 39 Preparation of CD4

3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanoic acid was mixed with EDCI (78 mg, 0.4 mmol) and cyclohexylamine in dichloromethane and the reaction mixture was stirred for 16 h to obtain N-cyclohexyl-3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanamide after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient.

Example 40 Preparation of CD48

Ethyl 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetate (0.1 g, 0.35 mmol) was taken in 4 ml aqueous ammonia and heated at 120 deg C. for 5 min in microwave. The solid product precipitated out after the reaction was filtered through a Buchner funnel and washed with 10% sodium bicarbonate (10 ml×2) followed by demineralised water (10 ml×2) wash. Product was vacuum dried and was taken in 5 ml ethanolic HCl, stirred for 15 min, concentrated in vacuo to afford 38 mg of 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetamide as hydrochloride salt. ¹H NMR (DMSO)HCl Salt 10.38 (bs, 1H), 7.67 (s, 1H), 7.58 (s, 1H), 7.43 (d, 1H), 7.38 (s, 1H), 7.18 (d, 1H), 4.79 (d, 2H), 4.62 (d, 1H), 4.21-4.31 (m, 1H), 3.68-3.81 (m, 1H), 3.42-3.53 (m, 1H), 3.04-3.14 (m, 2H), 2.96 (s, 3H).

Example 40A

A mixture of ethyl 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetate (100 mg) and piperidine (1 ml) was heated at 120° C. for 15 h to obtain 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)-1-(piperidin-1-yl)ethanone as TFA salt after purification by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05

Example 41 Preparation of CD14

2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetic acid was mixed with EDCI and benzyl alcohol and the reaction mixture was stirred for 16 h to obtain benzyl 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetate after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient. The free base was converted into its oxalate salt by treatment of oxalic acid (1 equiv) in anhydrous THF.

Example 42 Preparation of CD24

A mixture of ethyl 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetate (100 mg) and isopropylamine (1 ml) was heated at 120° C. for 15 h to obtain 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)-N-isopropylacetamide after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient. The free base was converted into its oxalate salt by treatment of oxalic acid (1 equiv) in anhydrous THF.

Example 43 Preparation of CD31

3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanoic acid was mixed with EDCI and cyclohexylmethanamine in dichloromethane and the reaction mixture was stirred for 16 h to obtain N-(cyclohexylmethyl)-3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanamide after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient. The free base was converted into its oxalate salt by treatment of oxalic acid (1 equiv) in anhydrous THF.

The compounds prepared according to the Examples are further detailed in Table 4.

TABLE 4 Synthetic Data HPLC Example Compound NMR MS HPLC RT No. No. Salt MW Solvent NMR Data Observed Method¹ (min) 1 CD1 Free 300.40 CDCl3 7.2 (s, 1H), 7.18 (d, 301 2 5.06 Base 1H), 7.0 (d, 1H), 4.3 (t, 2H), 4.1 (q, 2H), 3.7 (s, 2H), 2.9 (s, 4H), 2.7 (t, 2H), 2.6 (s, 3H), 2.4 (s, 3H), 1.25 (t, 3H) 2 CD6 Oxalate 404.46 DMSO 7.4 (d, 1H), 7.2 (s, 315 1 5.81 Salt 1H), 7.0 (d, 1H), 4.1 (t, 2H), 4.0 (q, 2H), 3.4 (m, 2H), 3.05 (m, 2H), 2.9 (s, 3H), 2.5 (m, 2H), 2.4 (s, 3H), 2.3 (t, 2H), 1.9 (m, 2H), 1.15 (t, 3H). 3  CD11 Free 306.79 CDCl3 7.4 (s, 1H), 7.05 (s, — — — Base 2H), 4.7 (s, 2H), 4.2 (q, 2H), 3.65 (s, 2H), 3.0-2.8 (m, 4H), 2.6 (s, 3H), 1.25 (t, 3H). 4  CD59 Free 320.82 CDCl3 7.65 (d, 1H), 7.3 (d, — — — Base 1H), 7.1 (d, 1H), 4.3 (t, 2H), 4.1 (q, 2H), 3.65 (s, 2H), 2.9 (s, 4H), 2.7 (t, 2H), 2.6 (s, 3H), 1.2 (t, 3H). 5  CD61 TFA 353.34 CDCl3 7.35-7.15 (m, 3H), 240 1 4.88 Salt 4.9 (m, 2H), 4.7 (m, 1H), 4.1 (m, 1H), 3.9 (m, 1H), 3.4 (m, 2H), 3.1 (m, 1H), 3.05 (s, 3H), 2.4 (s, 3H). 6 CD9 TFA 532.7782 CDCl3 7.25 (d, 1H), 7.2 (s, 318 1 6.22 Salt 1H), 7.05 (d, 1H), 5.65 (t, 1H), 4.65 (s, 2H), 4.6 (m, 1H), 4.4.3 (m, 1H), 4.2-4.0 (m, 2H), 3.8 (bs, 1H), 3.5 (m, 2H), 3.45-3.2 (m, 2H), 3.0 (s, 3H), 2.95 (m, 1H), 2.4 (s, 3H). 7  CD50 TFA 479.47 CDCl3 13.1 (bs, 1H), 8.2 366 1 5.77 Salt (s, 1H), 7.3 (m, 1H), 7.1-6.95 (m, 3H), 6.8 (t, 2H), 4.8-4.6 (m, 1H), 4.6-4.5 (m, 1H), 4.2 (m, 1H), 4.1 (m, 1H), 3.8 (m, 1H), 3.65 (m, 1H), 3.3 (m, 1H), 3.1 (m, 1H), 3.05 (s, 3H), 2.8-2.6 (m, 2H), 2.3 (s, 3H) 8 CD2 Free 285.39 CDCl3 7.2 (d, 1H), 7.15 (s, 286 1 4.42 Base 1H), 7.0 (d, 1H), 5.40 (bs, 1H), 4.4 (t, 2H), 3.8 (s, 2H), 3.0 (s, 4H), 2.65 (s, 3H), 2.55 (d, 3H), 2.5 (t, 2H), 2.4 (s, 3H). 9 CD3 Free 299.41 CDCl3 7.2 (m, 2H), 6.95 300 1 4.67 Base (d, 1H), 5.1 (bs, 1H), 4.35 (t, 2H), 3.65 (s, 2H), 3.1 (m, 2H), 2.85 (m, 4H), 2.55 (s, 3H), 2.5 (t, 2H), 2.4 (s, 3H), 0.9 (t, 3H). 10 CD5 Free 339.47 CDCl3 7.2 (m, 2H), 6.95 340 1 5.39 base (d, 1H), 5.05 (d, 1H), 4.35 (t, 2H), 4.0 (sext, 1H), 3.65 (s, 2H), 2.9-2.8 (m, 4H), 2.55 (s, 3H), 2.5 (t, 2H), 2.4 (s, 3H), 1.9-0.8 (t, 8H). 11 CD7 Free 313.44 CDCl3 7.2 (m, 2H), 7.0 (d, 314 1 4.94 base 1H), 5.3 (bs, 1H), 4.1 (t, 2H), 3.65 (s, 2H), 3.2 (m, 2H), 2.8 (m, 4H), 2.55 (s, 3H), 2.4 (s, 3H), 2.15-2.0 (m, 4H), 1.05 (t, 3H). 12  CD62 TFA 357.37 DMSO 7.35 (d, 1H), 7.2 (s, — — — Salt 1H), 7.0 (d, 1H), 4.25 (t, 2H), 4.0 (bs, 2H), 3.4 (bs, 2H), 3.0 (m, 4H), 2.8 (s, 3H), 2.3 (s, 3H). 13 CD8 TFA 568.642 CDCl3 mixture of rotamers 455 1 6.06 Salt 7.4-7.0 (m, 3H), 4.8-2.8 (m, 15H), 3.05 and 3.0 (s, 3H), 2.4 (s, 3H), 2.2 (s, 1H), 1.8-1.5 (m, 4H), 1.4 (s, 9H) 14  CD10 bis- 582.548 CDCl3 11.45 (bs, 1H), 355 1 3.93 TFA 10.05 (bs, 1H), 9.4 salt (bs, 1H), 7.4-7.0 (m, 3H), 6.6 (bs, 1H), 4.8-4.6 (m, 2H), 4.4-3.8 (m, 6H), 3.65-2.8 (m, 6H), 3.1 and 3.05 (s, 3H), 2.8-2.5 (m, 1H), 2.45 and 2.4 (s, 3H), 2.0-1.6 (m, 4H). 26  CD60 TFA 386.37 — — — — — Salt ¹Method-1 Column: YMC ODS-A 150 mm × 4.6 mm × 5μ, ID: E-AC-1/06/COL/013 Mobile Phase: A: 0.05% TFA in Water/B: 0.05% TFA in Acetonitrile Inj. Vol: 10 μL, Col. Temp.: 30° C., Flow rate: 1.4 mL/min Gradient: 5% B to 95% B in 8 min, Hold for 1.5 min, 9.51-12 min 5% B Method-2 Column: YMC ODS-A 150 mm × 4.6 mm × 5μ, ID: E-AC-1/06/COL/013 Mobile Phase: A: 0.05% TFA in Water/B: 0.05% TFA in Acetonitrile Inj. Vol: 10 μL, Col. Temp.: 30° C., Flow rate: 1.2 mL/min Gradient: 10% B to 80% B in 5 min, Hold for 2 min, 7.01-10 min 10% B

The compounds prepared according to the General Methods described herein and the synthetic procedures are further detailed below.

Example 44 Preparation of 3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)-1-methylpyrrolidin-2-one (Compound 71)

A suspension of NaH (36 mg, 1.5 mmol) and 2,3,4,5-tetrahydro-2,8-dimethyl-1H-pyrido[4,3-b]indole (100 mg, 0.5 mmol) in DMF (5 mL) was stirred at 0° C. 3-bromo-1-methylpyrrolidin-2-one (176 mg, 1.0 mmol) in DMF (3 mL) was added dropwise to the reaction mixture which was stirred at RT for 12 hours. After completion of the reaction, the reaction mixture was quenched with ice cold water and the product extracted with Ethyl Acetate. The organic layer isolated was washed with water and dried over sodium sulfate. The solvent was removed under reduced pressure and the crude obtained was purified by column chromatography to obtain 20 mg of 3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)-1-methylpyrrolidin-2-one. ¹H NMR (CDCl3) FREEBASE 7.10 (s, 1H), 7.05 (d, 1H), 6.92 (d, 1H), 5.05 (m, 1H), 4.80 (m, 1H), 3.80 (m, 1H), 3.50 (m, 2H), 3.40 (m, 1H), 3.20 (m, 3H), 3.0 (s, 3H), 2.80 (s, 3H), 2.40 (s, 3H), 2.20 (m, 2H).

Compound 70 (CD72) and Compound 72 are prepared according to the procedure for Compound 71 using the appropriate starting materials.

Example 45 Preparation of 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)cyclohexanol (Compound 73)

2,8-dimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (1 gm, 5 mmol) was taken in DMF (10 ml). NaH (300 mg, 12.5 mmol) was added to it and the reaction mixture stirred at RT for 15 min. 7-oxabicyclo[4.1.0]heptane (0.9 ml, 9.0 mmol) was taken in DMF (3 ml) and added drop wise to the reaction mixture. After complete addition, reaction mixture was heated at 60-65° C. overnight. The reaction was monitored by LCMS. After completion of the reaction, reaction mixture was cooled to RT and quenched with water, extracted with ethyl acetate (3×25 ml), dried over sodium sulfate and concentrated under vacuum to obtain the crude product. This crude was purified by silica gel column chromatography (Eluent: 20% Methanol in DCM) to get 900 mg of 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)cyclohexanol as yellow semi solid. ¹H NMR (CDCl3) FREE BASE 7.37-7.30 (m, 2H), 7.20 (s, 1H), 4.37-4.22 (bs, 1H), 3.67-3.64 (s, 1H), 3.61-3.57 (m, 2H), 3.0-2.80 (m, 3H), 2.60-2.40 (m, 7H), 1.98-1.82 (m, 4H), 1.50-1.38 (m, 4H).

Example 46 Preparation of 2,8-dimethyl-5-(prop-2-ynyl)-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (CD73)

p-Tolylhydrazine hydrochloride (600 mg, 3.7 mmol), propargyl bromide (80 wt % solution in toluene, 0.34 ml, 3.7 mmol), triethylamine (1.5 ml, 11.3 mmol) and N-methyl-4-piperidone hydrochloride (316 mg, 2.1 mmol) were taken in ethanol (15 ml) to obtain 80 mg of 2,3,4,5-tetrahydro-2,8-dimethyl-5-(prop-2-ynyl)-1H-pyrido[4,3-b]indole after purification on silica gel (230-400 mesh) chromatography, eluting with methanol-dichloromethane gradient. ¹H NMR (CDCl3) 7.30-7.25 (d, 1H), 7.20 (s, 1H), 7.00-6.90 (d, 1H), 4.80 (s, 2H), 3.70 (s, 2H), 2.95 (m, 4H), 2.60 (s, 3H), 2.40 (s, 3H), 2.10-2.00 (t, 1H).

Example 47 Preparation of N-benzyl-3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanamide (CD74)

Ethyl 3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl) propanoate (200 mg, 0.66 mmol) was added to benzylamine (2.0 ml, excess) and the reaction mixture was heated at 100° C. for 14 h. After completion of the reaction (monitored by LCMS) it was concentrated and basified with aqueous saturated sodium bicarbonate and extracted with ethyl acetate. The organic layer was concentrated to dryness and the crude obtained was purified by silica gel chromatography (Eluent: 10% MeOH in dichloromethane) to get 70 mg (yield: 29.16%) of N-benzyl-3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanamide as a free base. To the free base (40 mg, 0.11 mmol) dissolved in THF (5.0 ml), oxalic acid (13 mg, 0.10 mmol) in THF (5.0 ml) was added slowly, the mixture was stirred at RT for 20 minutes and the solid obtained was filtered, washed with ether and dried to get 35 mg (yield: 71.4%) of N-benzyl-3-(1,2,3,4-tetrahydro-2,8-dimethylpyrid[4,3-b]indol-5-yl)propanamide as oxalate salt. ¹H NMR (DMSO) 7.50-7.30 (t, 3H), 7.20-7.10 (m, 3H), 7.0-6.90 (m, 2H), 4.40-4.30 (m, 4H), 4.30-4.20 (t, 2H), 4.0 (s, 2H), 3.10 (m, 2H), 2.90 (s, 3H), 2.60-2.50 (t, 3H), 2.40 (s, 3H).

Example 48 Preparation of 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)-N-cyclohexylacetamide (CD75)

A solution of ethyl 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl) acetate (500 mg, 1.63 mmol) in oxalyl chloride (2.0 g, 16.33 mmol) was stirred at 25° C. for 3 h. After completion of the reaction (monitored by LCMS), cyclohexyl amine (1.0 ml, excess) was added to it and the reaction mixture heated at 80° C. for 3 h. The reaction mixture was concentrated and basified with aqueous saturated sodium bicarbonate and extracted with ethyl acetate. The organic layer was concentrated to dryness and the resulting crude was purified by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 ml) to obtain 10 mg (yield: 2.0%) of 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)-N-cyclohexylacetamide as TFA salt. ¹H NMR (DMSO) 10.0 (bs, 1H), 8.30 (d, 1H), 7.60 (s, 1H), 7.5 (d, 1H), 7.21 (d, 1H), 4.80 (m, 2H), 4.6 (m, 1H), 4.30 (m, 1H), 3.80 (m, 1H), 3.41 (m, 2H), 3.10 (bs, 2H), 3.0 (s, 3H), 1.80-1.20 (m, 10H).

Example 49 Preparation of N-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethyl)isobutyramide (CD76)

A mixture of 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethanamine (100 mg, 0.411 mmol), isobutyric acid (36 mg, 0.411 mmol), N,N′-dicyclohexylcarbodiimide (93 mg, 0.452 mmol) and 4-dimethylaminopyridine (55 mg, 0.452 mmol) in dry dichloromethane (5.0 ml) were stirred at room temperature for 4 h. The reaction mixture was filtered through Celite and concentrated using rotary evaporator to afford 16 mg of N-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethyl)isobutyramide as TFA Salt after purification by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 ml). ¹H NMR (DMSO) 9.95 (bs, 1H), 7.9 (t, 1H), 7.4 (d 1H), 7.2 (s, 1H), 7.0 (d, 1H), 4.5-4.61 (m, 1H), 4.1-4.28 (m, 3H), 3.7-3.9 (m, 2H), 3.1-3.2 (m, 2H), 2.95 (s, 3H), 2.4 (s, 3H), 2.19-2.3 (m, 1H), 1.2-1.38 (m, 2H), 0.9 (d, 6H).

Example 50 Preparation of N-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethyl)cyclohexanecarboxamide (CD77)

A mixture of 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethanamine (100 mg, 0.41 mmol), cyclohexane carboxylic acid (52 mg, 0.41 mmol), N,N′-dicyclohexylcarbodiimide (93 mg, 0.45 mmol) and 4-dimethylaminopyridine (55 mg, 0.45 mmol) in dry dichloromethane (2.5 ml) were stirred at room temperature for 3 h. The reaction mixture was filtered through Celite and concentrated using rotary evaporator to afford 10 mg of N-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethyl)cyclohexanecarboxamide as TFA salt after purification by reversed-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 ml). ¹H NMR (DMSO) 9.94 (bs, 1H), 7.86 (t, 1H), 7.38 (d, 1H), 7.11 (s, 1H), 7.0 (d, 1H), 4.56-4.63 (m, 1H), 4.22-4.29 (m, 1H), 4.08-4.13 (m, 3H), 3.72-3.81 (m, 3H), 3.08-3.14 (m, 3H), 2.97 (s, 3H), 2.38 (s, 3H), 1.95-2.0 (m, 1H), 1.50-1.84 (m, 5H), 1.02-1.2 (m, 4H).

Example 51 Preparation of 2-chloro-4-fluoro-N-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethyl)benzamide (CD78)

A mixture of 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethanamine (100 mg, 0.41 mmol), 2-chloro 4-fluoro benzoic acid (71.8 mg, 0.41 mmol), N,N′-dicyclohexylcarbodiimide (93 mg, 0.45 mmol) and 4-dimethylaminopyridine (55.22 mg, 0.45 mmol) in dry dichloromethane (2.5 ml) were stirred at room temperature for 3 h. The reaction mixture was filtered through Celite and concentrated by rotary evaporation to obtain 2.93 mg of 2-chloro-4-fluoro-N-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethyl)benzamide as TFA salt after purification by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 0.5 ml). ¹H NMR (DMSO) 10.0 (bs, 1H), 8.6 (t, 1H), 7.5 (d, 1H), 7.4 (d, 1H), 7.1-7.25 (m, 3H), 7.0 (d, 1H), 4.55-4.60 (m, 1H), 4.15-4.35 (m, 4H), 3.70-3.8 (m, 2H), 3.09-3.2 (m, 3H), 2.95 (s, 3H), 2.4 (s, 3H).

Example 52 Preparation of 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetamide (CD79)

Ethyl 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetate (0.5 g, 1.75 mmol) was taken in 4 ml aqueous ammonia and microwaved at 120° C. for 5 min using Initiator (Biotage Microwave). The solid product precipitated out after the reaction was filtered through Buchner funnel and washed with 10% sodium bicarbonate (10 ml×2) followed by demineralised water (10 ml×2) wash. Product was vacuum dried and was taken in 5 ml ethanolic HCl, stirred for 15 minutes, concentrated in vacuo to afford 13 mg of 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetamide as HCl salt. ¹H NMR (DMSO) 10.2 (bs, 1H), 7.62 (s, 1H), 7.21-7.3 (m, 3H), 6.9 (d, 1H), 4.75 (s, 2H), 4.45-4.51 (m, 1H), 4.21-4.25 (m, 1H), 3.12-3.17 (m, 4H), 2.97 (s, 3H), 2.19 (s, 3H).

Example 53 Preparation of tert-butyl 4-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethylcarbamoyl)piperidine-1-carboxylate and N-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethyl)piperidine-4-carboxamide (CD 80)

A mixture of 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethanamine (100 mg, 0.41 mmol), 1-(tert-butoxycarbonyl)piperidine-4-carboxylic acid (94 mg, 0.41 mmol), N,N′-dicyclohexylcarbodiimide (93 mg, 0.45 mmol) and 4-dimethylaminopyridine (55 mg, 0.45 mmol) in dry dichloromethane (2.5 ml) were stirred at room temperature for 3 h. The reaction mixture was filtered through Celite and concentrated using rotary evaporator to obtain 14 mg of tert-butyl 4-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethylcarbamoyl)piperidine-1-carboxylate after purification by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 ml). The compound obtained was taken in 3 ml of HCl in dioxane and stirred for 111 to obtain 5 mg of N-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethyl)piperidine-4-carboxamide as HCl Salt. ¹H NMR (DMSO) 10.78 (bs, 1H), 8.1 (bs, 1H), 7.40 (d, 1H), 7.2 (s, 1H), 7.05 (d, 1H), 4.6-4.2 (m, 1H), 4.3-4.2 (m, 1H), 4.2 (m, 2H), 4.0-3.8 (m, 3H), 3.35-3.05 (m, 4H), 3.0 (s, 3H), 2.95-2.8 (m, 2H), 2.4 (s, 3H), 2.3-2.2 (m, 1H), 2.1-2.00 (m, 1H), 1.8-1.6 (m, 4H).

Example 54 Preparation of 4-fluoro-N-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethyl)benzamide (CD81)

A mixture of 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethanamine (0.1 g, 0.41 mmol), 4-fluoro benzoic acid (57 mg, 0.41 mmol), N,N′-dicyclohexylcarbodiimide (93 mg, 0.45 mmol) and 4-dimethylaminopyridine (55 mg, 0.45 mmol) in dry dichloromethane (2.5 ml) were stirred at room temperature for 3 h. The reaction mixture was filtered through Celite and concentrated by rotary evaporation to obtain 19.22 mg of 4-fluoro-N-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethyl)benzamide as TFA salt after purification by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 ml). ¹H NMR (DMSO) 9.98 (bs, 1H), 8.72 (t, 1H), 7.80-7.84 (m, 2H), 7.45 (d, 1H), 7.25-7.30 (m, 2H), 7.20 (s, 1H), 7.0 (d, 1H), 4.50-4.59 (m, 1H), 4.17-4.30 (m, 2H), 3.73-3.80 (m, 2H), (3.50-3.59 (m, 3H), 3.05-3.15 (m, 2H), 2.92 (s, 3H), 2.37 (s, 3H).

Example 55 Preparation of 3-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanamide (CD82)

Ethyl 3-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanoate (0.1 g, 0.315 mmol) was taken in 4 ml aqueous ammonia and microwaved at 120° C. for 5 minutes. The solid product precipitated out after the reaction was filtered through Buchner funnel and washed with 10% sodium bicarbonate (10 ml×2) followed by demineralised water (10 ml×2) wash to obtain 1.25 mg of 3-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanamide as TFA salt after purification by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 ml). ¹H NMR (DMSO) 9.85 (bs, 1H), 7.5-7.6 (m, 2H), 7.4 (s, 1H), 7.2 (d, 1H), 6.85 (s, 1H), 4.6-4.7 (m, 2H), 4.4 (t, 2H), 3.7-3.8 (m, 2H), 3.1-3.2 (m, 4H), 3.0 (s, 3H).

Example 56 Preparation of N-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethyl)cyclopentanecarboxamide (CD83)

A mixture of 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethanamine (100 mg, 0.41 mmol), cyclopentane carboxylic acid (46 mg, 0.41 mmol), N,N′-dicyclohexylcarbodiimide (93 mg, 0.45 mmol) and 4-dimethylaminopyridine (55 m g, 0.45 mmol) in dry dichloromethane (2.5 ml) were stirred at room temperature for 3 h. The reaction mixture was filtered through Celite and concentrated to obtain 40 mg of N-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethyl)cyclopentanecarboxamide as TFA salt after purification by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 0.5 ml). ¹H NMR (DMSO) 9.98-10.09 (bs, 1H), 7.93 (t, 1H), 7.37 (d, 1H), 7.20 (s, 1H), 7.0 (d, 1H), 4.59-4.63 (m, 1H), 4.2-4.3 (m, 1H), 4.07-4.15 (m, 2H), 3.73-3.84 (m, 2H), 3.07-3.15 (m, 2H), 2.99 (s, 3H), 2.59-2.68 (m, 2H), 2.4-2.48 (m, 1H), 2.38 (s, 3H), 1.4-1.84 (m, 8H).

Example 57 Preparation of N-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethyl)-3-methylpyridine-4-carboxamide (CD84)

A mixture of 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethanamine (0.1 g, 0.411 mmol), 3-methylpyridine-4-carboxylic acid (0.056 g, 0.411 mmol), N,N′-dicyclohexylcarbodiimide (0.093 g, 0.452 mmol) and 4-dimethylaminopyridine (0.055 g, 0.452 mmol) in dry dichloromethane (2.0 ml) were stirred at room temperature for 4 h. To the reaction mixture was added 10 ml of water and the product extracted with dichloromethane (10 ml×3). Combined dichloromethane layers were dried over sodium sulfate and concentrated under reduced pressure to obtain 7 mg of N-(2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)ethyl)-3-methylpyridine-4-carboxamide as TFA salt after purification by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 ml). ¹H NMR (DMSO) 10.05 (bs, 1H), 8.7 (t, 1H), 8.45-8.55 (m, 2H), 7.4 (d, 1H), 7.22 (s, 1H), 7.15 (d, 1H), 7.0 (d, 1H), 4.6 (d, 1H), 3.72-3.85 (m, 3H), 3.4-3.6 (m, 3H), 3.1-3.2 (m, 3H), 3.0 (s, 3H), 2.4 (s, 3H), 2.2 (s, 3H).

Example 58 Preparation of 3-(8-chloro-2-methyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)propan-1-ol (CD87)

To a solution of 5-allyl-8-chloro-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (300 mg, 1.15 mmol, 1 equiv) in 6 ml of dry THF was added 0.5M 9-borabicyclo[3.3.1]nonane (2.54 ml, 1.26 mmol, 1.1 equiv) dropwise at RT. After 90 min, a second portion of 9-borabicyclo[3.3.1]nonane (2.3 ml, 1.15 mmol) was added and stirred for 16 h. It was quenched with 8 ml of 20% NaOH and 4 ml of 30% H2O2 solution at 5-10° C. under stiffing for 30 minutes. The reaction mixture was diluted with ethyl acetate (20 ml) followed by washing with brine, dried over sodium sulfate and concentrated under reduced pressure to obtain the crude product which was purified by preparative HPLC to give 3-(8-chloro-2-methyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)propan-1-ol as a TFA salt. ¹H NMR (DMSO) 10.0 (bs, 1H), 7.55-7.51 (m, 2H), 7.18-7.15 (m, 1H), 4.62-4.50 (m, 1H), 4.27-4.25 (m, 1H), 4.19-4.16 (t, 2H), 3.78 (bs, 1H), 3.36-3.34 (m, 3H), 3.16 (bs, 2H), 2.99 (s, 3H), 1.8-1.78 (t, 2H).

Example 59 Preparation of 5-(2-bromoethyl)-8-chloro-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (CD88)

A solution of 2-(8-chloro-2-methyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)ethanol (0.2 g, 0.75 mmol) in aqueous HBr (2 mL) was heated at 120° C. for 15 h. The reaction was monitored by TLC and LCMS. The reaction mixture was basified with solid sodium bicarbonate, extracted with ethyl acetate. Organic layer was dried over sodium sulfate and concentrated under reduced pressure to obtain crude product which was purified by silica gel (100-200 mesh) chromatography followed by preparative TLC to obtain 5 mg of 5-(2-bromoethyl)-8-chloro-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole as a free base. The free base (0.005 g 0.0152 mmol) was further dissolved in 2 mL of THF, oxalic acid (0.001 g, 0.015 mmol) in THF (1 mL) was added to it and the resulting mixture was stirred for 30 min at room temperature. The precipitate obtained was filtered and dried under vacuum to afford 1.5 mg of 5-(2-bromoethyl)-8-chloro-2,3,4,5-tetrahydro-2-methyl-1H-pyrido[4,3-b]indole as oxalate salt. ¹H NMR (CD₃OD) 7.55 (s, 1H), 7.5 (d, 1H), 7.2 (d, 1H), 4.6 (t, 2H), 4.5 (s, 2H), 3.8 (t, 2H), 3.7-3.6 (m, 2H), 3.3 (bs, 2H), 3.1 (s, 3H).

Example 60 Preparation of 2-(8-chloro-2-methyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)ethanol (CD89)

To a solution of lithium aluminum hydride (0.059 g, 1.5 mmol) in THF (30 mL) was added ethyl 2-(8-chloro-2-methyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)acetate (0.4 g, 1.3 mmol) in THF (10 mL) drop wise at 0° C. The reaction mixture was further heated at 100° C. for 6 h. Reaction was monitored by TLC and LCMS. On completion of the reaction, reaction mixture was quenched with H2O:NaOH:H2O (1:1:3) and the contents were filtered. The filtrate obtained was extracted with Ethyl acetate. Combined organic layers were dried over sodium sulfate and concentrated under reduced pressure to obtain crude product (300 mg). 100 mg of the crude was purified by preparative TLC to obtain 5 mg of 2-(8-chloro-2-methyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)ethanol as free base. The free base (0.015 g 0.056 mmol) was further dissolved in THF (2 mL), oxalic acid (0.007 g, 0.056 mmol) in THF (1 mL) was added to it and the resulting mixture was further stirred for 30 min at room temperature. The precipitate obtained was filtered and dried under vacuum to afford 20 mg of 2-(8-chloro-2-methyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)ethanol as an oxalate salt. ¹H NMR (CD3OD) 7.45 (s, 1H), 7.4 (d, 1H), 7.1 (d, 1H), 4.3 (s, 2H), 4.2 (t, 2H), 3.9 (t, 2H), 3.5 (t, 2H), 3.2 (t, 2H), 2.9 (s, 3H).

Example 61 Preparation of 2-(2,8-dimethyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)ethanol (CD90)

Lithium Aluminum Hydride (0.088 g, 2.3 mmol) was charged in dry THF (5 mL) and the contents cooled to 0° C. 2-(2,8-dimethyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)acetic acid (0.2 g, 0.77 mmol) was then added to it portion wise. The reaction mixture was refluxed overnight. The reaction mixture was cooled to 0° C. and quenched with aqueous sodium sulfate. The solid formed was filtered through Celite, washed with THF, dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain the crude product, which was then purified by column chromatography to give 2-(2,8-dimethyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)ethanol. 10 mg of it was taken in dry THF (2 mL), oxalic acid (5 mg) was added to it. The solvent was evaporated under reduced pressure to afford 0.1 g of 2-(2,8-dimethyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)ethanol as oxalate salt. ¹H NMR (DMSO) 7.4 (d, 1H), 7.2 (s, 1H), 7.0 (d, 1H), 4.4 (bs, 1H), 4.2 (s, 2H), 3.7 (bs, 2H), 3.2 (bs, 2H), 2.9 (s, 3H), 2.6-2.4 (m, 4H), 2.3 (s, 3H).

Example 62 Preparation of (2-bromoethyl)-2,8-dimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (CD91)

Aqueous HBr (0.9 ml, 10 times) was added to 2-(2,8-dimethyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)ethanol (0.09 g, 0.368 mole) and the contents heated to 120° C. for 10 hrs. The reaction mixture was cooled to 0° C. and basified with saturated NaOH Solution. The product was extracted with ethyl acetate, the combined organic layers were dried over anhydrous sodium sulfate and concentrated to obtain the crude product which was purified by preparative HPLC to get 5-(2-bromoethyl)-2,8-dimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole as TFA salt. ¹H NMR (CD3OD) 2.4, 3H(s); 3.15, 3H(s); 3.5-3.65, 2H (m); 3.7-3.8, 2H (t); 3.85-3.95, 2H (m); 4.3-4.4, 2H (m); 4.5-4.6, 2H (t); 7.05-7.1, 1H (d); 7.25-7.3, 1H(s); 7.35-7.4, 1H (d).

Example 63 Preparation of 3-(2,8-dimethyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)propanenitrile (CD92)

2,8-dimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (1.5 g, 7.5 mmol) was taken in 20 ml of benzene: toluene mixture (1:1) along with acrylonitrile (1 ml, 15 mmol), cooled to 0° C., followed by addition of triton base (0.3 ml). The contents were stirred for 15 min. Acrylonitrile and triton base (same amount) were added and stirred at RT for 1 h. The reaction was monitored by TLC and LCMS. On completion of the reaction, reaction mixture was quenched with water, extracted with ethyl acetate, dried over anhydrous sodium sulfate and evaporated under reduced pressure to obtain solid material, which was crystallized using diethyl ether to yield 3-(2,8-dimethyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)propanenitrile (yield: 1 g). ¹H NMR (CDCl3) 7.25 (s, 1H), 7.18-7.15 (d, 1H), 7.08-7.03 (d, 1H), 4.38-4.32 (t, 2H), 3.70-3.65 (m, 2H), 2.95-2.90 (m, 4H), 2.78-2.70 (t, 2H), 2.58 (s, 3H), 2.45 (s, 3H).

Example 64 Preparation of 3-(8-chloro-2-methyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)propanenitrile (CD94)

8-chloro-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (1.00 g, 4.5 mmol) was stirred in benzene (15 mL) and toluene (20 mL). To this solution acrylonitrile (0.5 mL, 7.5 mmol) was added. The resulting reaction mixture was stirred at 0° C. for 10 minutes. Ice cold solution of 1 ml of Triton-B® was added to it. The reaction mixture was again stirred at room temperature for 4 h. The reaction was monitored by TLC in 10% Methanol-dichloromethane. Water was added to the reaction mixture and extracted organic layer was given water wash (3 times). The organic layer was then concentrated and purified by silica gel (100-200 mesh) chromatography using 0-10% methanol:dichloromethane as eluent. The obtained 3-(8-chloro-2-methyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)propanenitrile was converted into its oxalate salt. ¹H NMR (DMSO) 7.65 (d, 1H), 7.55 (s, 1H), 7.20 (d, 1H), 4.50 (t, 2H), 4.30 (m, 2H), 3.40 (m, 2H), 3.20 (m, 2H), 3.0 (t, 2H), 2.90 (s, 3H).

Example 65 Preparation of CD12

Ethyl 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetate (100 mg, 0.32 mmol) was added to propan-2-ol (1.0 ml, excess) and the reaction mixture was heated at 100 deg C. for 14 h. After completion of the reaction (monitored by LCMS) reaction mixture was concentrated and basified with aqueous saturated sodium bicarbonate, extracted with ethyl acetate. The organic layer was concentrated to dryness and the crude obtained was purified by silica gel chromatography (Eluent: 10% MeOH in dichloromethane) to get 10 mg (yield: 10%) of isopropyl 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetate. The free base product (10 mg, 0.03 mmol) was dissolved in THF (1.0 ml), oxalic acid (4 mg, 0.03 mmol) in THF (1.0 ml) was added slowly, the mixture was stirred at RT for 20 minutes and the solid obtained was filtered, washed with ether and dried to get 10 mg (yield: 83%) of isopropyl 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl) acetate as oxalate salt. ¹H NMR (DMSO) OXALATE SALT 7.60 (s, 1H), 7.50 (d, 1H), 7.20 (d, 1H), 5.1 (s, 2H), 4.90 (m, 1H), 4.50 (m, 1H), 4.20 (m, 1H), 3.5 (m, 2H), 3.10 (bs, 2H), 3.0 (s, 3H), 1.10 (d, 6H).

Example 66 Preparation of CD13

A mixture of 8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indole-5-carboxylic acid (150 mg, 0.540 mmol), N,N′-dicyclohexylcarbodiimide (133 mg, 0.647 mmol) and 4-dimethylaminopyridine (99 mg, 0.810 mmol) in dry dichloromethane (4.0 ml) were stirred at room temperature for 15 minutes. To this reaction mixture was added t-butanol (48 mg, 0.647 mmol). The reaction mixture was stirred at room temperature for 18 h. The product was extracted with dichloromethane and washed with water. The combined organic layer was dried over sodium sulfate and concentrated to afford 85 mg of tert-butyl 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetate as TFA salt after purification by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 0.5 ml). ¹H NMR (DMSO) TFA SALT 10.1 (bs, 1H), 7.58 (d, 1H), 7.5 (d, 1H), 7.18 (d, 1H), 5.1 (dd, 2H), 4.65 (m, 1H), 4.3 (m, 1H), 3.8 (m, 1H), 3.5 (m, 1H), 3.02-3.14 (m, 2H), 2.9 (s, 3H), 1.2 (s, 9H).

Example 67 Preparation of CD15

To a solution of 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetic acid (200 mg, 0.7 mmol) and cyclohexyl methanol (80 mg, 0.7 mmol) in dichloromethane (10 ml) were added N,N′-dicyclohexylcarbodiimide (177 mg, 0.86 mmol) and 4-dimethylaminopyridine (105 mg, 0.86 mmol) and the contents were stirred at 25 deg C. for 16 h. The reaction mixture was concentrated to dryness to obtain the crude compound which was purified by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 ml) to give 30 mg (11.3%) of cyclohexylmethyl 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetate as TFA salt. ¹H NMR (DMSO) TFA SALT 10.39 (bs, 1H), 7.60 (s, 1H), 7.50 (d, 1H), 7.2 (d, 1H), 5.3-5.1 (dd, 2H), 4.70 (d, 1H), 4.30 (bs, 1H), 4.0 (d, 2H), 3.85 (bs, 1H), 3.50 (bs, 1H), 3.10 (s, 2H), 2.85 (s, 3H), 1.60-0.90 (m, 11H).

Example 68 Preparation of CD16

A mixture of 2-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)acetic acid (150 mg, 0.53 mmol), thionyl chloride (0.6 ml) and cyclopentanol (1.5 ml, 16.48 mmol) were heated at 90 deg C. for 3 h. After completion of the reaction (monitored by LCMS), solvent was removed in vacuo and purified by silica gel (230-400 mesh) chromatography, eluting with methanol-dichloromethane gradient to obtain 30 mg of title compound as free base. To a solution of title compound (30 mg, 0.08) in dry THF (5 ml) was added a solution of oxalic acid (11 mg, 0.08 mmol) in THF (2 ml) dropwise. The resulting mixture was stirred for 10 min and the solid obtained was filtered and dried to obtain 15 mg of title compound as oxalate salt. ¹H NMR (DMSO) OXALATE SALT 7.80 (s, 1H), 7.50-7.40 (d, 1H), 7.20-7.10 (d, 1H), 5.15 (bs, 1H), 5.1 (s, 2H), 4.3 (bs, 2H), 3.5 (bs, 2H), 3.05 (bs, 2H), 2.90 (s, 3H), 1.90-0.80 (m, 8H).

Example 69 Preparation of CD18

3-(8-Chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanoic acid (0.1 g, 0.34 mmol) in dichloromethane (3 ml) was cooled to 0° C. Oxalyl chloride (0.04 ml, 0.41 mmol) was added drop-wise to the reaction mixture. A catalytic amount (1 drop) of dimethyl formamide was added to the reaction mixture. Reaction mixture was stirred for 1 h at room temperature. Excess oxalyl chloride was distilled off under reduced pressure. To this residue, solution of isopropyl alcohol (0.028 ml, 0.374 mmol) in dichloromethane (2 ml) and 4-dimethylaminopyridine (0.055 g, 0.45 mmol) was added under nitrogen at room temperature and reaction mass was stirred for 30 min at room temperature. Reaction mixture was quenched with water and neutralized with 10% sodium bicarbonate, extracted with Ethyl acetate (10 ml×2). Combined organic layers dried over sodium sulfate and concentrated under reduced pressure to obtain crude product which was further purified by flash column chromatography using Methanol:dichloromethane (5:95) as eluent to afford 27 mg of product. This product was stirred in THF (2 ml) and oxalic Acid (10 mg, 0.080 mmol) for 15 min and the mixture was concentrated under vacuo to afford 31 mg. of isopropyl 3-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanoate as oxalate salt. ¹H NMR (DMSO) OXALATE SALT 7.60-7.50 (m, 2H), 7.20 (d, 1H), 4.80 (m, 1H), 4.40 (m, 4H), 3.4 (m, 1H), 3.8 (m, 1H), 3.4 (m, 2H), 2.90 (s, 3H), 2.70 (t, 2H), 1.10 (d, 6H).

Example 70 Preparation of CD20

3-(8-Chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanoic acid (0.1 g, 0.34 mmol) in dichloromethane (3 ml) was cooled to 0° C. Oxalyl chloride (0.04 ml, 0.41 mmol) was added drop-wise to the reaction mixture. A catalytic amount (1 drop) of dimethyl formamide was added to the reaction mixture. Reaction mixture was stirred for 1 h at room temperature. Excess oxalyl chloride was distilled off under reduced pressure. To this residue the solution of benzyl alcohol (0.038 ml, 0.374 mmol) in 2 ml dichloromethane and 4-dimethylaminopyridine (0.055 g, 0.45 mmol) were added under nitrogen at room temperature and reaction mixture was stirred for 30 minutes at room temperature. Reaction mixture was quenched with water and neutralized with 10% sodium bicarbonate, extracted with ethyl acetate (10 ml×2). Combined organic layers dried over sodium sulfate and concentrated under reduced pressure to obtain crude product which was further purified by flash column chromatography using Methanol:dichloromethane (5:95) as eluent to afford 23 mg of product. This product was stirred in THF (2 ml) and oxalic acid (7 mg, 0.06 mmol) for 15 min and mixture was concentrated under vacuo to afford 35 mg of benzyl 3-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanoate as oxalate salt. ¹H NMR (DMSO) OXALATE SALT 7.26 (d, 2H), 7.35-7.40 (m, 3H), 7.20-7.25 (m, 2H), 7.15 (d, 1H), 5.1 (s, 2H), 4.4 (m, 4H), 3.4 (m, 2H), 3.19-3.0 (m, 2H), 2.95 (s, 3H), 2.8 (m, 2H).

Example 71 Preparation of CD21

3-(8-Chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanoic acid (0.1 g, 0.34 mmol) was dissolved in dichloromethane (3 ml) and cooled to 0 deg C. Oxalyl chloride (0.04 ml, 0.41 mmol) was added drop-wise to the reaction mixture. A catalytic amount (1 drop) of dimethyl formamide was added to the reaction mixture. Reaction mixture was stirred for 1 h at room temperature. Excess oxalyl chloride was distilled off under reduced pressure. To this residue, solution of cyclohexyl methanol (0.046 ml, 0.374 mmol) in dichloromethane (2 ml) and 4-dimethylaminopyridine (0.055 g, 0.45 mmol) were added under nitrogen at room temperature and reaction mixture was stirred for 30 min at room temperature. Reaction mixture was quenched with water and neutralized with 10% sodium bicarbonate, extracted with Ethyl acetate (10 ml×2). Combined organic layers were dried over sodium sulfate and concentrated under reduced pressure to obtain crude product which was further purified by flash column chromatography using Methanol:dichloromethane (5:95) as eluent to afford −20 mg of product. This product was stirred in THF (2 ml) and oxalic acid (6 mg, 0.0515 mol) for 15 min and the mixture was concentrated under vacuo to afford 26 mg of cyclohexylmethyl 3-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanoate as oxalate salt. ¹H NMR (DMSO) OXALATE SALT 7.52-7.56 (m, 2H), 7.15 (d, 1H), 4.4 (t, 2H), 4.26 (bs, 2H), 3.80 (d, 2H), 3.50 (bs, 2H), 3.1 (bs, 2H), 2.90 (s, 3H), 2.80 (t, 2H), 1.70-0.807 (m, 11H).

Example 72 Preparation of CD22

3-(8-Chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanoic acid (0.1 g, 0.34 mmol) was dissolved in dichloromethane (3 ml) and cooled to 0 deg C. Oxalyl chloride (0.04 ml, 0.41 mmol) was added drop-wise to the reaction mixture. A catalytic amount (1 drop) of dimethyl formamide was added to the reaction mixture. Reaction mixture was stirred for 1 h at room temperature. Excess oxalyl chloride was distilled off under reduced pressure. To this residue, solution of cyclopentanol (0.034 g, 0.374 mmol) in 2 ml dichloromethane and 4-dimethylaminopyridine (0.055 g, 0.45 mmol) were added under nitrogen at room temperature and reaction mixture was stirred for 30 min at room temperature. Reaction mixture was quenched with water and neutralized with 10% sodium bicarbonate, extracted with Ethyl acetate (10 ml×2). Combined organic layers were dried over sodium sulfate and concentrated under reduced pressure to obtain crude product which was further purified by flash column chromatography using Methanol:dichloromethane (5:95) as eluent to afford 20 mg of product. This product was stirred in THF (2 ml) and oxalic acid (7 mg, 0.0555 mol) for 15 min and the mixture was concentrated under vacuo to afford 27 mg of cyclopentyl 3-(8-chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)propanoate as oxalate salt. ¹H NMR (DMSO) OXALATE SALT 7.4-7.6 (m, 2H), 7.2 (d, 1H), 5.0-5.10 (m, 2H), 4.35 (t, 2H), 3.8-3.2 (m, 5H), 2.9 (s, 3H), 2.8 (m, 2H), 1.8-1.9 (m, 3H), 1.4-1.6 (m, 5H).

Example 73 Preparation of CD49

Ethyl 3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanoate (0.1 g, 0.33 mmol) was taken in 4 ml aqueous ammonia and heated at 120 deg C. for 5 min using in microwave. The solid product precipitated out after the reaction was filtered through a Buchner funnel and washed with 10% sodium bicarbonate (10 ml×2) followed by demineralised water (10 ml×2) wash to obtain 1.25 mg of 3-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)propanamide as TFA salt after purification by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 ml). ¹H NMR (DMSO) TFA SALT 9.85 (bs, 1H), 7.4-7.45 (m, 2H), 7.2 (s, 1H), 7.0 (d, 1H), 6.85 (s, 1H), 4.3-4.2 (m, 3H), 3.6-3.4 (m, 2H), 3.2-3.1 (m, 2H), 3.0 (s, 3H), 2.7 (m, 2H), 2.3 (s, 3H).

Example 74 Preparation of CD25

To a solution of 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetic acid (200 mg, 0.77 mmol) in dichloromethane (20 ml) was added N,N′-dicyclohexylcarbodiimide (191 mg, 0.92 mmol) followed by the addition of 4-dimethylaminopyridine (113 mg, 0.93 mmol) and tert butylamine (67 mg, 0.93 mmol). The resulting mixture was stirred at 25 deg C. for 14 h. The solvent was removed in vacuo and purified by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 ml) to obtain 35 mg of N-tert-butyl-2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetamide as trifluoroacetic acid salt. ¹H NMR (DMSO-D2O) TFA SALT 7.21-7.20 (d, 2H), 7.0-6.95 (d, 1H), 4.60-4.50 (d, 2H), 3.75-3.65 (m, 2H), 3.50-3.38 (m, 2H), 3.10-3.0 (m, 2H), 2.90 (s, 3H), 2.30 (s, 3H), 1.20 (s, 9H).

Example 75 Preparation of CD27

p-Tolylhydrazine hydrochloride (500 mg, 3.16 mmol), 2-chloro-N-(cyclohexylmethyl)acetamide (600 mg, 3.16 mmol), triethylamine (1.31 ml, 9.4 mmol) and ethanol (20 ml) were stirred together to obtain 870 mg of 2-(1-p-tolylhydrazinyl)-N-(cyclohexylmethyl)acetamide. The intermediate (870 mg, 3.15 mmol) and N-methyl-4-piperidone hydrochloride (471 mg, 3.16 mmol) were taken in ethanolic HCl (20 ml) and stirred at RT for 15 min, after which the solvent was removed in vacuo. The reaction mixture obtained was taken in ethanol and heated at 90 deg C. for 14 h. After completion of the reaction (monitored by LCMS), the reaction mixture was concentrated to dryness and basified with aqueous saturated sodium bicarbonate, extracted with ethyl acetate. The organic layer was separated, dried over sodium sulfate and concentrated to obtain the crude product which was purified by silica gel chromatography (Eluent: 10% MeOH in dichloromethane) to yield 70 mg (yield: 6.27%) of N-(cyclohexylmethyl)-2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetamide. The freebase obtained (70 mg, 0.19 mmol) was dissolve d in THF (10.0 ml), oxalic acid (24 mg, 0.19 mmol) in THF (10.0 ml) was added slowly, the mixture was stirred at RT for 20 min and the solid obtained was filtered, washed with ether and dried to get 70 mg (yield: 80.4%) of N-(cyclohexylmethyl)-2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)acetamide as oxalate salt. ¹H NMR (DMSO-D2O) OXALATE SALT 8.3-8.2 (t, 1H), 7.30 (d, 1H), 7.2 (s, 1H), 7.0-6.9 (d, 1H), 4.70 (s, 2H), 4.3 (bs, 2H), 3.80-3.2 (m, 4H), 3.1 (bs, 2H), 2.90 (s, 3H), 2.30 (s, 3H), 1.70-1.50 (m, 5H), 1.40-1.30 (m, 1H), 1.20-1.0 (m, 4H), 0.90-0.70 (m, 1H).

Example 76 Preparation of CD29

To a solution of tert-butyl amine (1.0 gm, 13.6 mmol) in dichloromethane (50 ml) was added 3-chloropropionyl chloride (2.06 g, 16.3 mmol) and NaOH (650 mg, 16.25 in 2.0 ml H2O) solution simultaneously at −20 deg C. for 1 h. The reaction mixture was allowed to stir for 1 h at RT. The organic layer was washed with 5% HCl followed by 5% aqueous sodium bicarbonate. The organic layer was dried and concentrated to get 2.23 g (yield: 99%) N-tert-butyl-3-chloropropanamide as white solid. To a solution of p-Tolylhydrazine hydrochloride (500 mg, 3.16 mmol) in ethanol (15 ml) was added triethylamine (1.31 ml, 9.4 mmol) and N-tert-butyl-3-chloropropanamide (510 mg, 3.12 mmol). The resulting reaction mixture was heated at 90 deg C. for 14 hrs. The reaction mixture was concentrated to dryness and basified with aqueous saturated sodium bicarbonate, extracted with ethyl acetate. The organic layer was dried over sodium sulfate and concentrated to obtain the crude, which was purified by silica gel chromatography (Eluent: 10% MeOH in dichloromethane) to obtain 500 mg (yield: 63.3%) of 3-(1-p-tolylhydrazinyl)-N-tert-butylpropanamide. The amide obtained (500 mg, 2.0 mmol) and N-methyl-4-piperidone hydrochloride (298 mg, 2.0 mmol) were dissolved in ethanolic HCl (20 ml) and stirred at RT for 15 minutes. The solvent was removed in vacuo. The reaction mixture obtained was dissolved in ethanol and heated at 90 deg C. for 14 h. After completion of the reaction (monitored by LCMS), the reaction mixture was concentrated to dryness and basified with aqueous saturated sodium bicarbonate, extracted with ethyl acetate, the organic layer was dried over sodium sulfate and concentrated. The crude obtained was purified by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 ml) to obtain 10 mg (yield: 1.12%) of the desired product as TFA salt. ¹H NMR (DMSO-D2O) TFA SALT 7.30-7.25 (d, 1H), 7.20 (s, 1H), 7.0-6.95 (d, 1H), 4.5 (m, 1H), 4.30-4.15 (m, 3H), 3.70-3.65 (m, 1H), 3.50-3.30 (m, 1H), 3.20-3.10 (m, 2H), 2.90 (s, 3H), 2.50-2.40 (d, 2H), 2.30 (s, 3H), 1.10 (s, 9H).

Example 77 Determination of the Ability of Compounds of the Invention to Bind a Histamine Receptor Histamine H₁

To evaluate in radioligand binding assays the activity of compounds of the invention, human recombinant histamine H₁ receptor expressed in Chinese hamster ovary (CHO) cells (De Backer, M. D. et al., Biochem. Biophys. Res. Comm. 197(3):1601, 1993) in a modified Tris-HCl buffer (50 mM Tris-HCl, pH 7.4, 2 mM MgCl₂, 100 mM NaCl, 250 mM Sucrose) was used. Compounds of the invention were incubated with 1.2 nM [³H]Pyrilamine for 180 minutes at 25° C. Non-specific binding was estimated in the presence of 1 μM pyrilamine. Receptor proteins were filtered and washed, the filters were then counted to determine [³H]Pyrilamine specifically bound. Compounds were screened at 1 μM, using 1% DMSO as vehicle. Biochemical assay results are presented as the percent inhibition of specific binding in Table 5.

Histamine H₂

To evaluate in radioligand binding assays the activity of compounds of the invention, human recombinant histamine H₂ receptor expressed in Chinese hamster ovary (CHO) K1 cells (Ruat, M., Proc. Natl. Acad. Sci. USA. 87(5):1658, 1990) in a 50 mM Phosphate buffer, pH 7.4 was used. Compounds of the invention were incubated with 0.1 nM [¹²⁵I]aminopotentidine for 120 minutes at 25° C. Non-specific binding was estimated in the presence of 3 μM Tiotidine. Receptor proteins were filtered and washed, the filters were then counted to determine [¹²⁵I]Aminopotentidine specifically bound. Compounds were screened at 1 μM, using 1% DMSO as vehicle. Biochemical assay results are presented as the percent inhibition of specific binding in Table 5.

Histamine H₃

To evaluate in radioligand binding assays the activity of compounds of the invention, human recombinant histamine H₃ receptor expressed in Chinese hamster ovary (CHO-K1) cells (Yanai K et al. Jpn J. Pharmacol. 65(2): 107, 1994; Zhu Y et al. Mol. Pharmacol. 59(3): 434, 2001) in a modified Tris-HCl buffer (50 mM Tris-HCl, pH 7.4, 5 mM MgCl₂, 0.04% BSA) is used. Compounds of invention are incubated with 3 nM [³H]R(−)-α-Methylhistamine for 90 minutes at 25° C. Non-specific binding is estimated in the presence of 1 μM R(−)-α-Methylhistamine. Receptor proteins are filtered and washed, the filters are then counted to determine [³H] R(−)-α-Methylhistamine specifically bound. Compounds are screened at 1 μM or lower, using 1% DMSO as vehicle. Compounds of the invention are tested in this biochemical assay and percent inhibition of specific binding is determined. Biochemical assay results are presented as the percent inhibition of specific binding.

Example 78 Determination of the Ability of Compounds of the Invention to Bind a Imidazoline I₂ Receptor Central Imidazoline I₂

To evaluate in radioligand binding assays the activity of compounds of the invention, rat central imidazoline I₂ receptor obtained from Wistar Rat cerebral cortex (Brown, C. M. et al., Br. J. Pharmacol. 99:803, 1990) in a modified Tris-HCl buffer (50 mM Tris-HCl buffer, pH 7.4, 0.5 mM EDTA) was used. Compounds of the invention were incubated with 2 nM [³H]Idazoxan for 30 minutes at 25° C. Non-specific binding was estimated in the presence of 1 μM Idazoxan. Receptor proteins were filtered and washed, the filters were then counted to determine [³H]Idazoxan specifically bound. Compounds were screened at 1 μM or lower, using 1% DMSO as vehicle. Compounds of the invention were tested in this biochemical assay and percent inhibition of specific binding was determined. Biochemical assay results are presented as the percent inhibition of specific binding in Table 5.

TABLE 5 Binding data Compound Imidazoline I₂ Histamine Binding (1 μM) No. Central (1 μM) H₁ H₂ 1 18 34 8 2 8 52 5 3 27 2 23 4 54 60 20 5 53 96 48 6 52 46 0 7 47 −10 33 8 57 101 74 9 9 −2 −4 28 4 10 25 99 28 11 5 101 7 12 101 40 13 16 96 51 14 98 89 15 23 99 47 17 96 64 19 101 81 20 95 93 21 98 82 22 51 85 11 23 1 65 1 24 44 5 25 18 72 9 26 66 22 27 8 63 5 28 21 18 29 84 34 30 61 18 41 31 33 45 20 45 24 82 3 46 52 −5 47 47 90 53 48 18 73 4 49 58 82 5 50 24 47 9 51 12 85 8 52 14 98 23 53 51 12 59 64 60 5 60 6 50 3 61 40 32 13 62 42 63 39 63 41 86 35 64 16 62 −3 65 23 34 −7 66 66 49 67 70 −6 68 58 31 69 88 14 73 2 8 CD1  55 101 35 CD17 62 100 46 CD46 28 69 −3 CD47 3 25 16 CD55 3 22 −2 CD57 100 28 CD58 3 5 5 CD61 60 98 15 CD62 13 44 65 CD73 73 96 19 CD87 97 18 CD88 98 64 CD89 92 14 CD90 60 11 CD91 98 65 CD92 99 8 CD94 97 2

Example 79 Determination of the Ability of Compounds of the Invention to Bind an Adrenergic Receptor Adrenergic α_(1A)

To evaluate in radioligand binding assays the activity of compounds of the invention, rat adrenergic α_(1A) receptor obtained from Wistar Rat submaxillary glands (Michel, A. D. et al., Br. J. Pharmacol. 98:883, 1989) in a modified Tris-HCl buffer (50 mM Tris-HCl buffer, pH 7.4, 0.5 mM EDTA) was used. Compounds of the invention were incubated with 0.25 nM [³H]Prozosin for 60 minutes at 25° C. Non-specific binding was estimated in the presence of 10 μM phentolamine. Receptor proteins were filtered and washed, the filters were then counted to determine [³H]Prozosin specifically bound. Compounds of the invention were screened at 1 μM or lower, using 1% DMSO as vehicle. Compounds of the invention were tested in this biochemical assay and percent inhibition of specific binding was determined. Biochemical assay results are presented as the percent inhibition of specific binding in Table 6.

Adrenergic α_(1B)

To evaluate in radioligand binding assays the activity of compounds of the invention, rat adrenergic α_(1B) receptor obtained from Wistar Rat liver (Garcia-S'ainz, J. A. et al., Biochem. Biophys. Res. Commun. 186:760, 1992; Michel A. D. et al. Br. J. Pharmacol. 98:883, 1989) in a modified Tris-HCl buffer (50 mM Tris-HCl buffer, pH 7.4, 0.5 mM EDTA) was used. Compounds of the invention were incubated with 0.25 nM [³H]Prozosin for 60 minutes at 25° C. Non-specific binding was estimated in the presence of 10 μM phentolamine. Receptor proteins were filtered and washed, the filters were then counted to determine [³H]Prozosin specifically bound. Compounds were screened at 1 μM or lower, using 1% DMSO as vehicle. Compounds of the invention were tested in this biochemical assay and percent inhibition of specific binding was determined. Biochemical assay results are presented as the percent inhibition of specific binding in Table 6.

Adrenergic α_(1D)

To evaluate in radioligand binding assays the activity of compounds of the invention, human recombinant adrenergic α_(1D) receptor expressed in human embryonic kidney (HEK-293) cells (Kenny, B. A. et al. Br. J. Pharmacol. 115(6):981, 1995) in a 50 mM Tris-HCl buffer, pH 7.4, was used. Compounds of invention were incubated with 0.6 nM [³H]Prozosin for 60 minutes at 25° C. Non-specific binding was estimated in the presence of 10 μM phentolamine. Receptor proteins were filtered and washed, the filters were then counted to determine [³H]Prozosin specifically bound. Compounds were screened at 1 μM or lower, using 1% DMSO as vehicle. Biochemical assay results are presented as the percent inhibition of specific binding in Table 6.

Adrenergic α_(2A)

To evaluate in radioligand binding assays the activity of compounds of the invention, human recombinant adrenergic α_(2A) receptor expressed in insect Sf9 cells (Uhlen S et al. J Pharmacol Exp Ther. 271:1558, 1994) in a modified Tris-HCl buffer (50 mM Tris-HCl, pH 7.4, 12.5 mM MgCl₂, 2 mM EDTA) was used. Compounds of invention were incubated with 1 nM [³H]MK-912 for 60 minutes at 25° C. MK912 is (2S-trans)-1,3,4,5′,6,6′,7,12b-octahydro-1′,3′-dimethyl-spiro[2H-benzofuro[2,3-a]quinolizine-2,4′(1′H)-pyrimidin]-2′(3′H)-one hydrochloride Non-specific binding was estimated in the presence of 10 μM WB-4101 (2-(2,6-Dimethoxyphenoxyethyl)aminomethyl-1,4-benzodioxane hydrochloride). Receptor proteins were filtered and washed, the filters were then counted to determine [³H]MK-912 specifically bound. Compounds were screened at 1 μM or lower, using 1% DMSO as vehicle. Biochemical assay results are presented as the percent inhibition of specific binding in Table 6.

Adrenergic α_(2B)

To evaluate in radioligand binding assays the activity of compounds of the invention, human recombinant adrenergic α_(2B) receptor expressed in Chinese hamster ovary (CHO-K1) cells (Uhlen S et al. Eur. J. Pharmacol. 343(1):93, 1998) in a modified Tris-HCl buffer (50 mM Tris-HCl, pH 7.4, 12.5 mM MgCl₂, 1 mM EDTA, 0.2% BSA) was used. Compounds of the invention were incubated with 2.5 nM [³H]Rauwolscine for 60 minutes at 25° C. Non-specific binding was estimated in the presence of 10 μM Prozosin. Receptor proteins were filtered and washed, the filters were then counted to determine [³H]Rauwolscine specifically bound. Compounds were screened at 1 μM or lower, using 1% DMSO as vehicle. Biochemical assay results are presented as the percent inhibition of specific binding in Table 6.

Adrenergic α_(2C)

To evaluate in radioligand binding assays the activity of compounds of the invention, human recombinant adrenergic α_(2C) receptor expressed in insect Sf9 cells (Uhlen S et al. J Pharmacol Exp Ther. 271:1558, 1994) in a modified Tris-HCl buffer (50 mM Tris-HCl, pH 7.4, 12.5 mM MgCl₂, 2 mM EDTA) was used. Compounds of the invention were incubated with 1 nM [³H]MK-912 for 60 minutes at 25° C. Non-specific binding was estimated in the presence of 10 μM WB-4101. Receptor proteins were filtered and washed, the filters were then counted to determine [³H]MK-912 specifically bound. Compounds were screened at 1 μM or lower, using 1% DMSO as vehicle. Compounds of the invention were tested in this biochemical assay and percent inhibition of specific binding was determined. Biochemical assay results are presented as the percent inhibition of specific binding in Table 6.

Example 80 Determination of the Ability of Compounds of the Invention to Bind a Dopamine Receptor Dopamine D_(2L)

To evaluate in radioligand binding assays the activity of compounds of the invention, human recombinant dopamine D_(2L) receptor expressed in Chinese hamster ovary (CHO) cells (Grandy, D. K. et al. Proc. Natl. Acad. Sci. USA. 86:9762, 1989; Hayes, G. et al., Mol. Endocrinol. 6:920, 1992) in a modified Tris-HCl buffer (50 mM Tris-HCl, pH 7.4, 1.4 mM Ascorbic Acid, 0.001% BSA, 150 mM NaCl) was used. Compounds of the invention were incubated with 0.16 nM [³H]Spiperone for 120 minutes at 25° C. Non-specific binding was estimated in the presence of 10 μM Haloperidol. Receptor proteins were filtered and washed, the filters were then counted to determine [³H]Spiperone specifically bound. Compounds were screened at 1 μM or lower, using 1% DMSO as vehicle. Biochemical assay results are presented as the percent inhibition of specific binding in Table 6.

TABLE 6 Inhibition of ligand binding to aminergic G protein- coupled receptors by compounds of the invention Dopamine Compound Adrenergic (1 μM) (1 μM) No. α_(1A) α_(1B) α_(1D) α_(2A) α_(2B) α_(2C) D_(2L) 1 5 13 20 18 51 4 2 10 22 17 35 55 2 3 8 14 45 14 80 1 4 35 41 64 45 93 4 5 69 77 70 74 98 50 6 18 31 0 59 36 48 7 54 62 67 73 86 36 8 82 80 72 90 102 22 9 5 21 11 20 25 −8 2 10 50 40 71 12 11 38 25 69 10 12 13 12 45 23 13 55 73 97 38 14 72 79 103 31 15 58 67 95 26 17 73 90 106 13 19 83 86 106 31 20 90 95 103 19 21 88 95 103 35 22 23 40 58 −2 23 15 12 18 5 24 −4 10 13 3 25 22 2 38 −3 26 32 22 45 −4 27 18 12 35 −2 28 58 44 85 −1 29 74 78 79 2 30 73 74 104 7 31 61 37 91 9 45 12 16 18 7 46 7 44 46 4 47 80 73 96 −3 48 10 20 13 −6 49 18 83 76 9 50 37 38 70 7 51 29 22 82 19 52 58 38 89 22 53 62 54 86 −2 59 56 45 96 4 60 22 23 52 18 61 28 46 70 −3 62 64 40 92 5 63 56 65 98 7 64 20 9 40 2 65 11 17 12 7 66 76 70 107 −2 67 32 79 72 −1 68 66 62 84 1 69 30 25 39 4 73 6 11 −2 −3 CD1  79 42 54 62 95 42 CD17 70 87 99 22 CD46 10 13 35 3 CD47 6 17 24 4 CD55 14 −2 10 3 CD57 39 45 65 12 CD58 0 −7 −6 2 CD61 82 94 74 73 89 39 CD62 34 42 32 26 CD73 65 84 57 70 101 43 CD87 75 79 103 10 CD88 94 80 104 27 CD89 69 70 100 0 CD90 23 22 61 −8 CD91 88 86 102 15 CD92 78 76 94 3 CD94 74 73 86 1

Example 81 Determination of the Ability of Compounds of the Invention to Bind a Serotonin Receptor Serotonin (5-Hydroxytryptamine) 5-HT_(1A)

To evaluate in radioligand binding assays the activity of compounds of the invention, human recombinant serotonin (5-Hydroxytryptamine) 5-HT_(1A) receptor expressed in Chinese hamster ovary (CHO-K1) cells (Martin G R and Humphrey P P A. Neuropharmacol. 33:261, 1994; May J A, et al. J Pharmacol Exp Ther. 306(1): 301, 2003) in a modified Tris-HCl buffer (50 mM Tris-HCl, pH 7.4, 0.1% Ascorbic Acid, 0.5 mM EDTA, 10 mM MgSO₄) is used. Compounds of invention are incubated with 1.5 nM [³H]8-OH-DPAT for 60 minutes at 25° C. Non-specific binding is estimated in the presence of 10 μM Metergoline. Receptor proteins are filtered and washed, the filters are counted to determine [³H] 8-OH-DPAT specifically bound. Compounds are screened at 1 μM or lower, using 1% DMSO as vehicle. Compounds of the invention are tested in this biochemical assay and percent inhibition of specific binding is determined.

Serotonin (5-Hydroxytryptamine) 5-HT_(1B)

To evaluate in radioligand binding assays the activity of compounds of the invention, serotonin (5-Hydroxytryptamine) 5-HT_(1B) receptor from Wistar Rat cerebral cortex (Hoyer et al. Eur. J. Pharmacol. 118: 1, 1985; Pazos et al. Eur J. Pharmacol. 106: 531, 1985) in a modified Tris-HCl buffer (50 mM Tris-HCl, pH 7.4, 154 mM NaCl, 10 μM Pargyline, 30 μM Isoprenaline) is used. Compounds of invention are incubated with 10 pM [¹²⁵I]Cyanopindolol for 90 minutes at 37° C. Non-specific binding as estimated in the presence of 10 μM Serotonin (5-HT). Receptor proteins are filtered and washed, the filters are counted to determine [¹²⁵I]Cyanopindolol specifically bound. Compounds are screened at 1 μM or lower, using 1% DMSO as vehicle. Compounds of the invention are tested in this biochemical assay and percent inhibition of specific binding is determined.

Serotonin (5-Hydroxytryptamine) 5-HT_(2A)

To evaluate in radioligand binding assays the activity of compounds of the invention, human recombinant serotonin (5-Hydroxytryptamine) 5-HT_(2A) receptor expressed in Chinese hamster ovary (CHO-K1) cells (Bonhaus, D. W. et al. Br. J. Pharmacol. 115:622, 1995; Saucier, C. and Albert, P. R., J. Neurochem. 68:1998, 1997) in a 50 mM Tris-HCl buffer, pH 7.4, was used. Compounds of the invention were incubated with 0.5 nM [³H]Ketanserin for 60 minutes at 25° C. Non-specific binding was estimated in the presence of 1 μM Mianserin. Receptor proteins were filtered and washed, the filters were then counted to determine [³H]Ketanserin specifically bound. Compounds were screened at 1 μM or lower, using 1% DMSO as vehicle. Biochemical assay results are presented as the percent inhibition of specific binding in Table 7.

Serotonin (5-Hydroxytryptamine) 5-HT_(2B)

To evaluate in radioligand binding assays the activity of compounds of the invention, human recombinant serotonin (5-Hydroxytryptamine) 5-HT_(2B) receptor expressed in Chinese hamster ovary (CHO-K1) cells (Bonhaus, D. W. et al., Br. J. Pharmacol. 115:622, 1995) in a modified Tris-HCl buffer (50 mM Tris-HCl, pH 7.4, 4 mM CaCl₂, 0.1% Ascorbic Acid) was used. Compounds of invention were incubated with 1.2 nM [³H]Lysergic acid diethylamide (LSD) for 60 minutes at 37° C. Non-specific binding was estimated in the presence of 10 μM Serotonin (5-HT). Receptor proteins were filtered and washed, the filters were then counted to determine [³H]LSD specifically bound. Compounds were screened at 1 μM or lower, using 1% DMSO as vehicle. Compounds of the invention were tested in this biochemical assay and percent inhibition of specific binding was determined. Biochemical assay results are presented as the percent inhibition of specific binding in Table 7.

Serotonin (5-Hydroxytryptamine) 5-HT_(2C)

To evaluate in radioligand binding assays the activity of compounds of the invention, human recombinant serotonin (5-Hydroxytryptamine) 5-HT_(2C) receptor expressed in Chinese hamster ovary (CHO-K1) cells (Wolf, W. A. and Schutz, J. S., J. Neurochem. 69:1449, 1997) in a modified Tris-HCl buffer (50 mM Tris-HCl, pH 7.4, 0.1% Ascorbic Acid, 10 μM Pargyline) was used. Compounds of the invention were incubated with 1 nM [³H]Mesulergine for 60 minutes at 25° C. Non-specific binding was estimated in the presence of 1 μM Mianserin. Receptor proteins were filtered and washed, the filters were then counted to determine [³H]Mesulergine specifically bound. Compounds were screened at 1 μM or lower, using 1% DMSO as vehicle. Biochemical assay results are presented as the percent inhibition of specific binding in Table 7.

Serotonin (5-Hydroxytryptamine) 5-HT₃

To evaluate in radioligand binding assays the activity of compounds of the invention, human recombinant serotonin (5-Hydroxytryptamine) 5-HT₃ receptor expressed in human embryonic kidney (HEK-293) cells (Miller K et al. Synapase. 11:58, 1992; Boess F G et al. Neuropharmacol. 36:637, 1997) in a modified Tris-HCl buffer (50 mM Tris-HCl, pH 7.4, 1 mM EDTA, 5 mM MgCl₂) is used. Compounds of invention are incubated with 0.69 nM [³H]GR-65630 for 60 minutes at 25° C. Non-specific binding is estimated in the presence of 10 μM MDL-72222. Receptor proteins are filtered and washed, the filters are counted to determine [³H]GR-65630 specifically bound. Compounds are screened at 1 μM or lower, using 1% DMSO as vehicle. Compounds of the invention are tested in this biochemical assay and percent inhibition of specific binding is determined.

Serotonin (5-Hydroxytryptamine) 5-HT₄

To evaluate in radioligand binding assays the activity of compounds of the invention, serotonin (5-Hydroxytryptamine) 5-HT₄ receptor from Duncan Hartley derived Guinea pig striatum (Grossman C J et al. Br J. Pharmacol. 109:618, 1993) in a 50 mM Tris-HCl, pH 7.4, is used. Compounds of invention are incubated with 0.7 nM [³H]GR-113808 for 30 minutes at 25° C. Non-specific binding is estimated in the presence of 30 μM Serotonin (5-HT). Receptor proteins are filtered and washed, the filters are counted to determine [³H]GR-113808 specifically bound. Compounds are screened at 1 μM or lower, using 1% DMSO as vehicle. Compounds of the invention are tested in this biochemical assay and percent inhibition of specific binding is determined.

Serotonin (5-Hydroxytryptamine) 5-HT_(5A)

To evaluate in radioligand binding assays the activity of compounds of the invention, human recombinant serotonin (5-Hydroxytryptamine) 5-HT_(5A) receptor expressed in Chinese hamster ovary (CHO-K1) cells (Rees, S. et al., FEBS Lett. 355:242, 1994) in a modified Tris-HCl buffer (50 mM Tris-HCl, pH 7.4, 10 mM MgCl₂, 0.5 mM EDTA) was used. Compounds of the invention were incubated with 1.7 nM [³H]Lysergic acid diethylamide (LSD) for 60 minutes at 37° C. Non-specific binding was estimated in the presence of 100 μM Serotonin (5-HT). Receptor proteins were filtered and washed, the filters were then counted to determine [³H]LSD specifically bound. Compounds were screened at 1 μM or lower, using 1% DMSO as vehicle. Compounds of the invention were tested in this biochemical assay and percent inhibition of specific binding was determined. Biochemical assay results are presented as the percent inhibition of specific binding in Table 7.

Serotonin (5-Hydroxytryptamine) 5-HT₆

To evaluate in radioligand binding assays the activity of compounds of the invention, human recombinant serotonin (5-Hydroxytryptamine) 5-HT₆ receptor expressed in human HeLa cells (Monsma, F. J. Jr. et al., Mol. Pharmacol. 43:320, 1993) in a modified Tris-HCl buffer (50 mM Tris-HCl, pH 7.4, 150 mM NaCl, 2 mM Ascorbic Acid, 0.001% BSA) was used. Compounds of the invention were incubated with 1.5 nM [3H]Lysergic acid diethylamide (LSD) for 120 minutes at 37° C. Non-specific binding was estimated in the presence of 5 μM Serotonin (5-HT). Receptor proteins were filtered and washed, the filters were then counted to determine [3H]LSD specifically bound. Compounds were screened at 1 μM or lower, using 1% DMSO as vehicle. Biochemical assay results are presented as the percent inhibition of specific binding in Table 7.

Serotonin (5-Hydroxytryptamine) 5-HT₇

To evaluate in radioligand binding assays the activity of compounds of the invention, human recombinant serotonin (5-Hydroxytryptamine) 5-HT_(S) receptor expressed in Chinese hamster ovary (CHO) cells (Roth, B. L. et al., J. Pharmacol. Exp. Ther. 268:1403, 1994; Shen, Y. et al., J. Biol. Chem. 268:18200, 1993) in a modified Tris-HCl buffer (50 mM Tris-HCl, pH 7.4, 10 mM MgCl₂, 0.5 mM EDTA) was used. Compounds of invention were incubated with 5.5 nM [³H] Lysergic acid diethylamide (LSD) for 2 hours at 25° C. Non-specific binding was estimated in the presence of 10 μM Serotonin (5-HT). Receptor proteins were filtered and washed, the filters were then counted to determine [³H]LSD specifically bound. Compounds were screened at 1 μM or lower, using 1% DMSO as vehicle. Biochemical assay results are presented as the percent inhibition of specific binding in Table 7.

TABLE 7 Inhibition of ligand binding to aminergic G protein- coupled receptors by compounds of the invention Compound Serotonin (1 μM) No. 5-HT_(2A) 5-HT_(2B) 5-HT_(2C) 5-HT_(5A) 5-HT₆ 5-HT₇ 1 30 23 20 4 8 33 2 22 20 −5 14 19 47 3 63 21 29 35 19 36 4 53 40 36 47 28 59 5 91 77 96 62 88 95 6 30 21 45 25 23 43 7 42 31 23 44 3 4 8 99 64 99 60 83 75 9 15 −5 29 −6 −5 −8 10 92 69 11 71 66 12 81 83 67 13 91 101 14 103 94 106 15 94 96 17 84 91 99 19 95 96 100 20 102 88 93 21 98 100 100 22 81 27 23 37 3 24 9 21 6 25 61 58 26 89 54 34 27 28 13 28 17 35 47 29 96 73 43 30 93 18 31 76 34 45 52 5 46 33 65 11 47 90 63 48 37 12 49 47 24 50 35 −1 51 70 30 52 85 83 53 39 51 22 59 72 22 60 35 22 61 27 10 62 54 19 63 72 31 64 45 5 65 24 3 66 98 93 35 67 55 65 24 68 77 40 15 69 30 24 −4 73 50 52 7 5 CD1  89 54 93 39 78 85 CD17 96 101 CD46 30 39 CD47 25 11 CD55 11 −3 CD57 92 96 67 CD58 −19 −5 CD61 77 43 73 52 68 94 CD62 28 12 CD73 87 94 92 63 83 91 CD87 66 79 35 CD88 98 84 87 CD89 70 84 36 CD90 58 91 7 CD91 96 98 88 CD92 67 61 47 CD94 60 71 40

Example 82 Determination of Serotonin (5-Hydroxytryptamine) 5-HT₂ Agonist/Antagonist Activity of Compounds of the Invention

To determine for agonist or antagonist activity of a test compound e.g. a compound of the invention, in functional assays, human recombinant serotonin 5-HT_(2A) receptor expressed in human embryonic kidney (HEK-293) cells (Jerman J C, Brough S J, Gager T, Wood M, Coldwell M C, Smart D and Middlemiss D N. Eur J Pharmacol, 414: 23-30, 2001) is used. Cells are suspended in DMEM buffer, and distributed in microplates. A cytoplasmic calcium fluorescent indicator which varies proportionally to the free cytosolic Ca²⁺ ion concentration is mixed with probenicid in HBSS buffer complemented with 20 mM Hepes (pH 7.4), added into each well and equilibrated with the cells for 30 min at 37° C. followed by 30 min at 22° C.

To measure agonist effects, a test compound, reference agonist or HBSS buffer (basal control) is added to the cells and changes in fluorescence intensity are measured using a microplate reader. For stimulated control measurements, 5-HT at 100 nM is added in separate assay wells.

The results are expressed as a percent of the control response to 100 nM 5-HT. The standard reference agonist is 5-HT, which is tested in each experiment at several concentrations to generate a concentration-response curve from which its EC₅₀ value is calculated.

To measure antagonist effects, the addition of the test compound, reference antagonist or HBSS buffer is followed by the addition of 3 nM 5-HT or HBSS buffer (basal control) prior the fluorescence measurements. The results are expressed as a percent inhibition of the control response to 3 nM 5-HT. The standard reference antagonist is ketanserin, which is tested in each experiment at several concentrations to generate a concentration-response curve from which its IC₅₀ value is calculated. Compounds are screened at 3 μM or lower, using DMSO as vehicle.

Example 83 Determination of Serotonin (5-Hydroxytryptamine) 5-HT₆ Agonist/Antagonist Activity of Compounds of the Invention

To determine for agonist or antagonist activity of a test compound, e.g., a compound of the invention in functional assays, human recombinant 5-HT₆ receptor is transfected in CHO cells (Kohen, R., Metcalf, M. A., Khan, N., Druck, T., Huebner, K., Lachowicz, J. E., Meltzer, H. Y., Sibley, D. R., Roth, B. L. And Hamblin, M. W. Cloning, characterisation and chromosomal localization of a human 5-HT6 serotonin receptor, J. Neurochem., 66: 47, 1996) and the activity of the test compound is determined by measuring their effects on cAMP production using the Homogeneous Time Resolved Fluorescence (HTRF) detection method. Cells are suspended in HBSS buffer complemented with HEPES 20 mM (pH 7.4) and 500 μM IBMX, and then distributed in microplates and incubated for 45 min at 37° C. in the absence (control) or presence of a test compound or the reference agonist or antagonist.

For agonist determinations, stimulated control measurement, separate assay wells contain 10 μM 5-HT. Following incubation, the cells are lysed and the fluorescence acceptor (D2-labeled cAMP) and fluorescence donor (anti-cAMP antibody labeled with europium cryptate) are added. After 60 min at room temperature, the fluorescence transfer is measured at lex=337 nm and lem=620 and 665 nm using a microplate reader. The cAMP concentration is determined by dividing the signal measured at 665 nm by that measured at 620 nm (ratio).

The results are expressed as a percent of the control response to 10 μM 5-HT. The standard reference agonist is 5-HT, which is tested in each experiment at several concentrations to generate a concentration-response curve from which its EC₅₀ value is calculated.

For antagonist determinations, the reference agonist 5-HT is added at a final concentration of 100 nM. For basal control measurements, separate assay wells do not contain 5-HT. Following 45 min incubation at 37° C., the cells are lysed and the fluorescence acceptor (D2-labeled cAMP) and fluorescence donor (anti-cAMP antibody labeled with europium cryptate) are added.

After 60 min at room temperature, the fluorescence transfer is measured as mentioned above. The results are expressed as a percent inhibition of the control response to 100 nM 5-HT. The standard reference antagonist is methiothepin

Example 84 Determination of Dopamine D_(2L) Antagonist Activity of Compounds

To determine for agonist or antagonist activity of a test compound, e.g. a compound of the invention, in functional assays, human recombinant dopamine D_(2L) receptor stably expressed in Chinese hamster ovary (CHO) cells (Senogles S E et al. J. Biol. Chem. 265(8): 4507, 1990) is used. The test compound is pre-incubated with the membranes (0.1 mg/ml) and 10 mM GDP in modified HEPES buffer (20 mM HEPES, pH 7.4, 100 mM NaCl, 10 mM MgCl₂, 1 mM DTT, 1 mM EDTA) for 20 minutes and Scintillation Proximity Assay (SPA) beads are added for another 60 minutes at 30° C. The reaction is initiated by 0.3 nM [³⁵S]GTPγS for an additional 15 minute incubation period. Increase of [³⁵S]GTPγS binding by 50 percent or more (350%) relative to the 1 mM dopamine response by the test compound indicates possible dopamine D_(2L) receptor agonists activity. Inhibition of a 10 μM dopamine-induced increase of [³⁵S]GTPγS binding response by 50 percent or more (350%) by the test compound indicated receptor antagonist activity. Compounds are screened at 3 μM or lower, using 0.4% DMSO as vehicle. Assay results are presented as the percent response of specific binding.

Example 85 Determination of Dopamine D_(2S) Antagonist Activity of Compounds

To determine for agonist or antagonist activity of a test compound, e.g. a compound of the invention, in functional assays, human recombinant dopamine D_(2S) receptor stably expressed in Chinese hamster ovary (CHO) cells (Gilliland S L and Alper R H. Naunyn-Schmiedeberg's Archives of Pharmacology. 361: 498, 2000) is used. The test compound is pre-incubated with the membranes (0.05 mg/ml) and 3 μM GDP in modified HEPES buffer (20 mM HEPES, pH 7.4, 100 mM NaCl, 10 mM MgCl₂, 1 mM DTT, 1 mM EDTA) for 20 minutes and Scintillation Proximity Assay (SPA) beads are then added for another 60 minutes at 30° C. The reaction is initiated by 0.3 nM [³⁵S]GTPγS for an additional 30 minute incubation period. Increase of [³⁵S]GTPγS binding by 50 percent or more (350%) relative to the 100 μM dopamine response by the test compound indicates possible dopamine D_(2S) receptor agonists activity. Inhibition of a 3 μM dopamine-induced increase of [³⁵S]GTPγS binding response by 50 percent or more (350%) by the test compound indicated receptor antagonist activity. Compounds are screened at 3 μM or lower, using 0.4% DMSO as vehicle. Assay results are presented as the percent response of specific binding.

Example 86 Determination for Agonist or Antagonist Activity of Compounds in a Histamine H₁ Functional Assay

To determine for agonist or antagonist activity of a test compound, e.g. a compound of the invention, in functional assays, human recombinant Histamine H₁ receptor expressed in human embryonic kidney (HEK-293) cells (Miller, T. R., Witte, D. G., Ireland, L. M., Kang, C. H., Roch, J. M., Masters, J. N., Esbenshade, T. A And Hancock, A. A. J. Biomol. Screen., 4: 249-258, 1999) is used. Cells are suspended in DMEM buffer, and then distributed in microplates. A cytoplasmic calcium fluorescent indicator, which varies proportionally to the free cytosolic Ca²⁺ ion concentration, is mixed with probenicid in HBSS buffer complemented with 20 mM Hepes (pH 7.4) and is then added into each well and equilibrated with the cells for 30 min at 37° C. and then for another 30 min at 22° C. To measure agonist effects, compounds of the invention, reference agonist or HBSS buffer (basal control) are added to the cells and changes in fluorescence intensity are measured using a microplate reader. For stimulated control measurements, histamine at 10 μM is added in separate assay wells.

The results are expressed as a percent of the control response to 10 μM histamine. The standard reference agonist is histamine, which is tested in each experiment at several concentrations to generate a concentration-response curve from which its EC₅₀ value is calculated.

To measure antagonist effects, the addition of the test compound, reference antagonist or HBSS buffer is followed by the addition of 300 nM histamine or HBSS buffer (basal control) prior the fluorescence measurements. The results are expressed as percent inhibition of the control response to 300 nM histamine. The standard reference antagonist is ketanserin, which is tested in each experiment at several concentrations to generate a concentration-response curve from which its IC₅₀ value is calculated. Compounds are screened at 3 μM or lower, using DMSO as vehicle.

Example 87 Increase of Neurite Outgrowth of Neurons that are Cultured with a Test Compound Neurite Outgrowth in Cortical Neurons

Compounds are tested to determine their ability to stimulate neurite outgrowth of cortical neurons. Standard methods are used to isolate cortical neurons. For the isolation of primary rat cortical neurons, the fetal brain from a pregnant rat at 17 days of gestation is prepared in Leibovitz's medium (L15; Gibco). The cortex is dissected out, and the meninges are removed. Trypsin (Gibco) is used to dissociate cortical C with DNAse I. The cells are triturated for 30 minutes with a pipette in Dulbecco's Modified Eagle Media (“DMEM”; Gibco) with 10% Fetal Bovine Serum (“FBS”) (Gibco) and centrifuged at 350×g for 10 minutes at room temperature. The cells are suspended in Neurobasal medium supplemented with 2% B27 (Gibco) and 0.5 mM L-glutamine (Gibco). The cells are maintained at 30,000 cells per well of poly-L-lysine coated plates at 37° C. in 5% CO₂-95% air atmosphere. After adhesion, a vehicle control or a test compound, e.g. a compound of the invention, are added at different concentrations to the medium. BDNF (50 ng/mL) is used as a positive control for neurite growth. After treatment, cultures are washed in phosphate-buffered saline (“PBS”; Gibco) and fixed in glutaraldehyde 2.5% in PBS. Cells are fixed after 3 days growth. Several pictures (˜80) of cells with neurites are taken per condition with a camera. The length measurements are made by analysis of the pictures using software from Image-Pro Plus (France). The results are expressed as mean (s.e.m.). Statistical analysis of the data is performed using one way analysis of variance (ANOVA).

Neurite Outgrowth in Rat Mixed Cortical Cultures

Cortical mixed cultures are prepared from Et 8 Wistar rat embryos. The cortices are dissected out and the tissue is cut to small pieces. The cells are separated by 15-min incubation with DNase and papain. The cells are collected by centrifugation (1500 rpm, 5 min). The tissue is triturated with a pipette and the cells are plated using the micro-islet protocol (20 000 cells in 25 μl medium) on poly-L-lysine coated 48 wells, in MEM supplemented with 2 mM glutamine, 0.1 μg/ml gentamicin, 10% heat-inactivated fetal bovine serum (FBS-HI) and 10% heat-inactivated horse serum (HS-HI). After the cells had attached to the well, 250 μl medium is added to the wells. Four hours after plating the medium is changed to fresh medium (MEM with supplements and 5% HS-HI) containing test compound at 0.5, 5 and 50 nM concentrations. As positive controls BDNF (50, 100 and/or 150 ng/ml), and/or NGF (50 ng/ml and/or 100 ng/ml) are used. After 2 days in vitro, the cell's conditioned media are collected from plates before fixing the cells. The media samples are centrifuged 13 000 rpm 3 min to get rid of cell debris. The samples are stored at −20 C for later analysis. Cells are formaldehyde-fixed and processed for immunocytochemistry. BDNF levels in the conditioned media are determined with a BDNF ELISA using the manufacturers (Promega, BDNF Emax® ImmunoAssay System, catalog number: G7610) instructions.

The cultures are fixed with 4% formaldehyde in 0.01 M PBS for 30 min and washed once with PBS. The fixed cells are first permeabilized and non-specific binding is blocked by a 30-min incubation with blocking buffer containing 1% bovine serum albumin and 0.3% Triton X-100 in PBS. Rabbit anti-MAP-2 (dilution 1:1000, AB5622, Chemicon, in blocking buffer) is used as a primary antibody. The cells are incubated with the primary antibody for 48 h at +4° C., washed with PBS and incubated with secondary antibody goat anti-rabbit IgG conjugated to Alexa Fluor568 (1:200, A11036, Molecular Probes) for 2 h at RT. The immunopositive cells are visualized by a fluorescence microscope equipped with appropriate filter set, and documented by a high resolution image capturing. The number of cells per field (4 field per well) are counted, and the neurite outgrowth is quantified using Image Pro Plus software.

The number of wells per compound concentration used is 6 (n=6). All data are presented as mean±standard deviation (SD) or standard error of mean (SEM), and differences are considered to be statistically significant at the p<0.05 level. Statistical analysis is performed using StatsDirect statistical software. Differences between group means are analyzed by using 1-way-ANOVA followed by Dunnet's test (comparison to the vehicle treated group).

Example 88 Use of an In Vivo Model to Evaluate the Ability of Compounds to Enhance Cognition, Learning and Memory in Scopolamine Treated Rats

The two-trial object recognition paradigm developed by Ennaceur and Delacour in the rat is used as a model of episodic memory. Ennaceur, A., and Delacour, J. (1988), Behav. Brain Res. 31:47-59. The paradigm is based on spontaneous exploratory activity of rodents and does not involve rule learning or reinforcement. The object recognition paradigm is sensitive to the effects of ageing and cholinergic dysfunction. See, e.g., Scali, C., et al. (1994), Neurosci. Lett. 170:117-120; and Bartolini, L., et al. (1996), Biochem. Behav. 53:277-283.

Male Sprague-Dawley rats between six and seven weeks old, weighing between 220-300 grams are obtained from Centre d'Elevage (Rue Janvier, B. P. 55, Le Genest-Saint-Isle 53940, France). The animals are housed in groups of 2 to 4 in polypropylene cages (with a floor area of 1032 cm²) under standard conditions: at room temperature (22±2° C.), under a 12 hour light/12 hour dark cycle, with food and water provided ad libitum. Animals are permitted to acclimate to environmental conditions for at least 5 days before therapy began, and are numbered on their tails with indelible marker.

The experimental arena is a square wooden box (60 cm×60 cm×40 cm) painted dark blue, with 15 cm×15 cm black squares under a clear plexiglass floor. The arena and objects placed inside the arena are cleaned with water between each trial to eliminate any odor trails left by rats. The arena is placed in a dark room illuminated only by halogen lamps directed towards the ceiling in order to produce a uniformly dim light in the box of approximately 60 lux. The day before testing, animals are allowed to freely explore the experimental arena for three minutes in the presence of two objects (habituation). Animals to be tested are placed in the experimental room at least 30 minutes before testing.

On the day of the experiment, animals are submitted to two trials separated by an interval of 120 minutes. During the first, or acquisition, trial (T₁), rats are placed in the arena, which is prepared with two identical objects. The time required for each animal to complete 15 seconds of object exploration is determined, with a cut-off time of four minutes. Exploration is considered to be directing the nose at a distance less than 2 centimeters (“cm”) from the object and/or touching the object. During the second, or testing, trial (T₂), one of the objects presented in the first trial is replaced with an unknown or novel object, while the second, familiar object is left in place. Rats are placed back in the arena for three minutes, and exploration of both objects is determined. Locomotor activity of rats (number of times rats cross grid lines visible under the clear plexiglass floor) is scored for during T₁ and T₂. At the conclusion of the experiments, the rats are sacrificed by an overdose of pentobarbital given intraperitoneally.

The following parameters are measured: (1) time required to achieve 15 seconds of object exploration during T₁; (2) locomotor activity during T₁ (number of crossed lines); (3) time spent in active exploration of the familiar object during T₂ (T_(Familiar)); (4) time spent in active exploration of the novel object during T₂ (T_(Novel)); and (5) locomotor activity during T₂ (number of crossed lines). The difference between time spent in active exploration of the novel object during T₂ and time spent in active exploration of the familiar object during T₂ (ΔT_(Novel)−T_(Familiar)) is evaluated. The % of animals in each group with T_(Novel)−T_(Familiar) greater than or equal to 5 seconds is also derived; described as % of good learners.

Animals not meeting a minimal level of object exploration are excluded from the study as having naturally low levels of spontaneous exploration. Thus, only rats exploring the objects for at least five seconds (T_(Novel)+T_(Familiar)>5 seconds) are included in the study.

Animals are randomly assigned to groups of 14. A test compound, e.g. a compound of the invention, and controls are administered to animals the groups as follows: Solutions of compounds are prepared freshly each day at a concentration of 0.25 mg/ml using purified water or saline as vehicle. Donepezil, used as a positive control, and scopolamine are administered simultaneously in a single solution of saline (5 mL/kg) prepared freshly each day. Scopolamine is purchased from Sigma Chemical Co. (Catalog No.S-1875; St. Quentin Fallavier, France) is dissolved in saline to a concentration of 0.06 mg/mL.

Donepezil or its vehicle and scopolamine are administered intraperitoneally forty minutes before the acquisition trial (T₁). Compounds or their vehicle are administered by gavage twenty-five minutes before the acquisition trial (T₁), i.e., five minutes after administration of scopolamine. The volume of administration is 5 ml/kg body weight for compounds administered intraperitoneally, and 10 ml/kg for compounds administered orally. Recognition scores and % of good learners is determined.

Example 89 Use of an In Vivo Model to Determine the Ability of Compounds to Treat, Prevent and/or Delay the Onset and/or the Development of Schizophrenia in PCP Treated Animals

In vivo models of schizophrenia can be used to determine the ability of the compounds described herein to treat and/or prevent and/or delay the onset and/or the development of schizophrenia.

One exemplary model for testing the activity of one or more compounds described herein to treat and/or prevent and/or delay the onset and/or development of schizophrenia employs phencyclidene, which is administered to the animal (e.g., non-primate (rat) or primate (monkey)), resulting in dysfunctions similar to those seen in schizophrenic humans. See Jentsch et al., 1997, Science 277:953-955 and Piercey et al., 1988, Life Sci. 43(4):375-385). Standard experimental protocols may be employed in this or in other animal models. One protocol involves PCP-induced hyperactivity.

Male C57Bl/6J mice from Jackson Laboratories (Bar Harbor, Me.) are used. Mice are received at 6-weeks of age. Upon receipt, mice are assigned unique identification numbers (tail marked) and are group-housed with 4 mice/cage in OPTI mouse ventilated cages. All animals remained housed in groups of four during the remainder of the study. All mice are acclimated to the colony room for at least two weeks prior to testing and are subsequently tested at an average age of 8 weeks of age. During the period of acclimation, mice are examined on a regular basis, handled, and weighed to assure adequate health and suitability. Animals are maintained on a 12/12 light/dark cycle. The room temperature is maintained between 20 and 23° C. with a relative humidity maintained between 30% and 70%. Food and water are provided ad libitum for the duration of the study. In each test, animals are randomly assigned across treatment groups.

The open filed (OF) test assesses locomotor behavior. The open field chambers are Plexiglas square chambers (27.3×27.3×20.3 cm; Med Associates Inc., St Albans, Vt.) surrounded by infrared photo beams (16×16×16) to measure horizontal and vertical activity. The analysis is configured to divide the open field into a center and periphery zone. Distance traveled is measured from horizontal beam breaks as the mouse moved whereas rearing activity is measured from vertical beam breaks.

Mice (10 to 12 animals per treatment group) are brought to the activity experimental room for at least 1 hr acclimation to the experimental room conditions prior to testing. Eight animals are tested in each run. The vehicle (10% DMSO or 5% PEG200 and 1% Tween 80), or the test compound dissolved in 5% PEG200, 1% Tween80 is administered orally 30 min prior to PCP injection. Clozapine (1 mg/kg) is dissolved in 10% DMSO and administered i.p. 30 min prior to PCP injection. The mice are placed in the OF chambers for 30 min following which either water or PCP (5 mg/kg) dissolved in sterile injectable water and administered i.p. and placed back in the OF chambers for a 60-minute session. At the end of each OF test session the OF chambers are thoroughly cleaned.

Data are analyzed by analysis of variance (ANOVA) followed by post-hoc comparisons with Fisher Tests when appropriate. Baseline activity is measured during the first 30 min of the test prior to PCP injection. PCP-induced activity is measured during the 60 min following PCP injection. Statistical outliers that fell above or below 2 standard deviations from the mean are removed from the final analyses. An effect is considered significant if p<0.05. Total distances traveled and total rearing for the test compound is determined.

In an alternative method, the protocol is as described above with the exception of the treatment groups which are as follows: all injections are at a dose volume of 10 ml/kg. The test compound is dissolved in Phosphate Buffered Saline (PBS) and administered orally 30 min prior to PCP injection. Clozapine (0.5 and 1.0 mg/kg) is dissolved in 10% DMSO and administered i.p. 30 min prior to Phencyclidine (PCP) injection. PCP (5.0 mg/kg) is dissolved in sterile injectable water and administered i.p. Total distances traveled for the test compound is determined.

Example 90 Use of an In Vivo Model to Determine the Ability of Compounds to Treat, Prevent and/or Delay the Onset and/or the Development of Schizophrenia in Amphetamine Treated Animals

Male C57Bl/6J mice from appropriate supplier (for example Jackson Laboratories, Bar Harbor, Me.) are used. Mice typically are received at 6-weeks of age. Mice are acclimated to the colony room for at least two weeks prior to testing. During the period of acclimation, mice are examined on a regular basis, handled, and weighed to assure adequate health and suitability and maintained on a 12/12 light/dark cycle. The room temperature is maintained between 20 and 23° C. with a relative humidity maintained between 30% and 70%. Food and water are provided ad libitum for the duration of the study. In each test, animals are randomly assigned between treatment groups.

The open field test (OF) is used to assess motor activity. The open field chambers are plexiglass square chambers (e.g., 27.3×27.3×20.3 cm; Med Associates Inc., St Albans, Vt.) surrounded by infrared photobeam sources (16×16×16). The enclosure is configured to split the open field into a center and periphery zone and the photocell beams are set to measure activity in the center and in the periphery of the OF chambers. Horizontal activity (distance traveled) and vertical activity (rearing) are measured from consecutive beam breaks.

On the day of testing, animals are brought to the experimental room for at least 1 hr acclimation prior to start of treatment. Animals are administered with vehicle, clozapine or test compound and placed in the OF. The time of administration of client compound to each animal is recorded. Baseline activity is recorded for 30 min following which mice receive amphetamine (4 mg/kg) or water placed back in the OF chambers for a 60-minute session. At the end of each open field test session the OF chambers are thoroughly cleaned. Typically ten to twelve mice are tested in each group. Test compound doses typically range from 0.01 mg/kg to 50 mg/kg.

Data are analyzed by analysis of variance (ANOVA) followed by post-hoc comparisons where appropriate. An effect is considered significant if p<0.05. Data are represented as the mean and standard error to the mean (s.e.m.)

Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, it is apparent to those skilled in the art that certain minor changes and modifications will be practiced. Therefore, the description and examples should not be construed as limiting the scope of the invention. 

1-36. (canceled)
 37. A compound of the Formula (E):

or a salt thereof, wherein: R¹ is H, hydroxyl, nitro, cyano, halo, substituted or unsubstituted C₁-C₈ alkyl, substituted or unsubstituted C₂-C₈ alkenyl, substituted or unsubstituted C₂-C₈ alkynyl, perhaloalkyl, acyl, acyloxy, carbonylalkoxy, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted aralkyl, C₁-C₈ perhaloalkoxy, alkoxy, aryloxy, carboxyl, thiol, thioalkyl, substituted or unsubstituted amino, acylamino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, aminosulfonyl, sulfonylamino, sulfonyl or carbonylalkylenealkoxy; each R^(2a) and R^(2b) is independently H, substituted or unsubstituted C₁-C₈ alkyl, halo, cyano, hydroxyl, alkoxy, nitro or R^(2a) and R^(2b) are taken together with the carbon to which they are attached to form a cycloalkyl moiety or a carbonyl moiety; each R^(3a) and R^(3b) is independently H, substituted or unsubstituted C₁-C₈ alkyl, halo, cyano hydroxyl, alkoxy, nitro or R^(3a) and R^(3b) are taken together with the carbon to which they are attached to form a cycloalkyl moiety or a carbonyl moiety; each X⁷, X⁸, X⁹ and X¹⁰ is independently N or CR⁴, provided that at least one of X⁷, X⁸, X⁹ and X¹⁰ is N; m and q are independently 0 or 1; n is 1; each R⁴ is independently H, hydroxyl, nitro, cyano, halo, C₁-C₈ perhaloalkyl, substituted or unsubstituted C₁-C₈ alkyl, substituted or unsubstituted C₂-C₈ alkenyl, substituted or unsubstituted C₂-C₈ alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, C₁-C₈ perhaloalkoxy, C₁-C₈ alkoxy, aryloxy, carboxyl, thiol, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aralkyl, thioalkyl, substituted or unsubstituted amino, acylamino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, aminosulfonyl, sulfonylamino, sulfonyl, carbonylalkylenealkoxy, alkylsulfonylamino or acyl; each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) is independently H, hydroxyl, substituted or unsubstituted alkyl or is taken together with the carbon to which it is attached and a geminal R^(8(a-f)) to form a cycloalkyl moiety; each R^(10a) and R^(10b) is independently H, substituted or unsubstituted C₁-C₈ alkyl, halo, hydroxyl, alkoxy or R^(10a) and R^(10b) are taken together with the carbon to which they are attached to form a cycloalkyl moiety or a carbonyl moiety; and Q is acyclic or cyclic acylamino, carbonylalkoxy, acyloxy, aminoacyl, or aminocarbonylalkoxy; provided that the compound is other than a compound selected from the group consisting of compounds: 5H-Pyrrolo[2,3-c:4,5-c′]dipyridine-5-acetamide, 1,2,3,4-tetrahydro-2-(1-methylethyl)-(Compound No. 107x); 5H-Pyrrolo[2,3-c:4,5-c′]dipyridine-5-acetamide, N-cyclohexyl-1,2,3,4-tetrahydro-2-(1-methylethyl)—(Compound No. 108x); 5H-Pyrrolo[3,2-c:4,5-c′]dipyridine-5-acetamide, 1,2,3,4-tetrahydro-2-(1-methylethyl)—(Compound No. 109x); and 5H-Pyrrolo[3,2-c:4,5-c′]dipyridine-5-acetamide, N-cyclohexyl-1,2,3,4-tetrahydro-2-(1-methylethyl)—(Compound No. 110x); and salts thereof.
 38. The compound of claim 37, or a salt thereof, wherein if each m and q is 0, R^(8e) and R^(8f) are H, and each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H, then R¹ is other than isopropyl.
 39. The compound of claim 37, or a salt thereof, wherein R¹ is other than isopropyl.
 40. The compound of claim 37, or a salt thereof, wherein one of X⁷, X⁸, X⁹ and X¹⁰ is N and three of X⁷, X⁸, X⁹ and X¹⁰ are CR⁴.
 41. The compound of claim 37, or a salt thereof, wherein two of X⁷, X⁸, X⁹ and X¹⁰ is N and two of X⁷, X⁸, X⁹ and X¹⁰ are CR⁴.
 42. The compound of claim 37, or a salt thereof, wherein X⁹ is N.
 43. The compound of claim 42, or a salt thereof, wherein R¹ is substituted C₁-C₈ alkyl, or unsubstituted C₁-C₈ alkyl other than isopropyl.
 44. The compound of claim 43, or a salt thereof, wherein R¹ is methyl.
 45. The compound of claim 42, or a salt thereof, wherein each X⁷, X⁸ and X¹⁰ is CH.
 46. The compound of claim 42, or a salt thereof, wherein each R^(2a), R^(2b), R^(3a), R^(3b), R^(10a) and R^(10b) is H.
 47. The compound of claim 42, or a salt thereof, wherein q is 0 and m is
 1. 48. The compound of claim 42, or a salt thereof, wherein Q is acyclic acylamino, aminoacyl or carbonylalkoxy.
 49. The compound of claim 37, or a salt thereof, wherein Q is acyclic acylamino other than —C(O)NMe₂ and —C(O)NH₂.
 50. The compound of claim 37, or a salt thereof, wherein Q is aminoacyl of the formula —NHC(O)R′ where R′ is alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclyl, substituted heterocyclyl, alkoxy or substituted alkoxy.
 51. The compound of claim 50, or a salt thereof, wherein R′ is substituted heteroaryl.
 52. The compound of claim 37, or a salt thereof, wherein X⁷ is N.
 53. The compound of claim 52, or a salt thereof, wherein the compound is of the formula (IIIg):


54. The compound of claim 53, or a salt thereof, wherein each R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f), where present, is independently H, hydroxyl, unsubstituted C₁-C₄ alkyl or is taken together with the carbon to which it is attached and a geminal R^(8(a-f)) to form a cycloalkyl moiety.
 55. The compound of claim 54, or a salt thereof, wherein q, m, R^(8a), R^(8b), R^(8c), R^(8d), R^(8e) and R^(8f) are taken together to form a moiety selected from the group consisting of: —CH₂—, —CH₂CH₂—, —CH₂CH₂CH₂—, —CH₂—C(H)(OH)—, —C(H)(OH)—CH₂—, —CH₂—C(OH)(CH₃)—, —C(OH)(CH₃)—CH₂—, —CH₂—C(H)(CH₃)—, —C(H)(CH₃)—CH₂—, —CH₂—C(CH₃)(CH₃)—, —C(CH₂CH₂)—CH₂— and —CH₂—C(CH₂CH₂)—.
 56. The compound of claim 53, or a salt thereof, wherein R⁴ is H, halo, unsubstituted C₁-C₄ alkyl, C₁-C₄ perhaloalkyl, or substituted or unsubstituted aryl.
 57. The compound of claim 53, or a salt thereof, wherein Q is acyclic acylamino, carbonylalkoxy or aminoacyl.
 58. The compound of claim 53, or a salt thereof, wherein Q is aminoacyl.
 59. The compound of claim 58, or a salt thereof, wherein Q is aminoacyl of the formula —NR_(a)C(O)R_(b) where R_(a) is H or alkyl and R_(b) is alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic or substituted heterocyclic.
 60. The compound of claim 59, or a salt thereof, wherein R_(a) is H.
 61. The compound of claim 60, or a salt thereof, wherein R_(b) is substituted or unsubstituted heteroaryl.
 62. A pharmaceutical composition comprising a compound according to claim 37 or a salt thereof, and a pharmaceutically acceptable carrier.
 63. A method of treating a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder or a neuronal disorder in an individual comprising administering to an individual in need thereof an effective amount of compound according to claim 37 or a salt thereof.
 64. A kit comprising a compound according to claim 37 or a salt thereof, and instructions for use in the treatment of a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder or a neuronal disorder. 